| NCT07044674 | A Cataract Surgery Clinical Trial | NOT_YET_RECRUITING | NA | 2026-02 | 2026-06 | 2026-05 |
| NCT07054281 | UNITY VCS Vitreoretinal Surgery | NOT_YET_RECRUITING | NA | 2026-01 | 2027-02 | 2026-10 |
| NCT07147192 | Feasibility Study of an Accommodating IOL Design | NOT_YET_RECRUITING | NA | 2025-11 | 2027-09 | 2027-01 |
| NCT06592521 | OPTI-FREE Family STUDY | WITHDRAWN | NA | 2025-10 | 2026-01 | 2026-01 |
| NCT07161635 | Post Market Clinical Evaluation of Clareon PanOptix Pro and Clareon PanOptix Pro Toric IOLs | NOT_YET_RECRUITING | NA | 2025-10 | 2026-10 | 2026-10 |
| NCT06588400 | AOSEPT (CLEAR CARE) PLUS Study | WITHDRAWN | NA | 2025-10 | 2026-01 | 2026-01 |
| NCT07082816 | Reformulated PG324 Ophthalmic Solution for Intraocular Pressure Reduction | RECRUITING | PHASE3 | 2025-09-02 | 2026-05 | 2026-05 |
| NCT07036835 | Clinical Investigation of a Femtosecond Laser for Corneal Flap Creation | RECRUITING | NA | 2025-08-27 | 2026-11 | 2026-11 |
| NCT06541795 | Evaluation of AcrySof IQ Vivity Extended Vision Intraocular Lenses | WITHDRAWN | NA | 2025-06 | 2026-12 | 2026-12 |
| NCT06884202 | Evaluation of Delefilcon A Contact Lenses | COMPLETED | NA | 2025-04-28 | 2025-08-26 | 2025-08-26 |
| NCT06784063 | Visual Performance With Clareon® Vivity® Intraocular Lenses (IOLs) | COMPLETED | NA | 2025-04-10 | 2025-06-13 | 2025-06-13 |
| NCT06571656 | Evaluation of the Safety and Tolerability of Ocular Lubricants | TERMINATED | NA | 2025-04-02 | 2025-07-11 | 2025-07-11 |
| NCT06660290 | A Study to Evaluate 0.003% AR-15512 Safety and Drop Attributes | COMPLETED | PHASE3 | 2025-01-15 | 2025-02-06 | 2025-02-06 |
| NCT06517316 | Cosmetic Contact Lenses Post-Market Clinical Follow-up Study | WITHDRAWN | NA | 2025-01 | 2026-03 | 2026-03 |
| NCT06493383 | Lotrafilcon B Plano Cosmetic Contact Lenses Study | WITHDRAWN | NA | 2025-01 | 2026-05 | 2026-05 |
| NCT06565624 | Evaluation of Reflex Tear Production | TERMINATED | NA | 2024-10-17 | 2024-11-07 | 2024-11-07 |
| NCT06544707 | A Study Designed to Evaluate Tear Production | COMPLETED | PHASE3 | 2024-10-15 | 2025-01-30 | 2025-01-30 |
| NCT06544694 | A Study to Investigate the Effect of 0.003% AR-15512 on Subjects With Dry Eye Disease | COMPLETED | PHASE3 | 2024-10-08 | 2025-03-21 | 2025-03-21 |
| NCT06538662 | An Investigation of FID 123320 for the Reduction of Ocular Redness in Pediatric and Adult Populations | COMPLETED | PHASE3 | 2024-10-07 | 2025-04-03 | 2025-01-27 |
| NCT06441643 | Next Generation Rocklatan | ACTIVE_NOT_RECRUITING | PHASE2 | 2024-09-04 | 2025-11 | 2025-11 |
| NCT06444516 | Study of Safety and Performance of a Novel Ocular Lubricant in Subjects With Dry Eye Disease | COMPLETED | NA | 2024-09-04 | 2025-02-07 | 2025-02-07 |
| NCT06444529 | A Double-Masked Comparison of FID 123320 Ophthalmic Solution to Vehicle for the Reduction of Ocular Redness | COMPLETED | PHASE3 | 2024-08-21 | 2025-01-08 | 2024-11-14 |
| NCT06461455 | Clinical Performance Evaluation of Two Frequent Replacement Silicone Hydrogel Multifocal Toric Contact Lenses | COMPLETED | NA | 2024-07-26 | 2024-12-31 | 2024-12-31 |
| NCT06469242 | Clinical Performance of Two Frequent Replacement Silicone Hydrogel Multifocal Contact Lenses | COMPLETED | NA | 2024-07-18 | 2024-10-08 | 2024-10-08 |
| NCT06400745 | Clareon PanOptix Pro vs. Clareon PanOptix - Study A | COMPLETED | NA | 2024-06-18 | 2025-04-30 | 2024-12-13 |
| NCT06401551 | Clareon PanOptix Pro vs. Clareon PanOptix - Study B | COMPLETED | NA | 2024-06-18 | 2025-04-30 | 2024-12-13 |
| NCT06166901 | Evaluation of Long-term Safety and Performance of PanOptix Intraocular Lens (IOLs) | COMPLETED | NA | 2024-04-27 | 2025-02-05 | 2025-02-05 |
| NCT06285695 | Clareon Toric Study (T2-T9) | ACTIVE_NOT_RECRUITING | NA | 2024-04-10 | 2028-07 | 2028-07 |
| NCT06165744 | Next Generation Cataract and Vitreoretinal Surgery Study | COMPLETED | NA | 2024-02-27 | 2024-08-19 | 2024-05-23 |
| NCT06165627 | Comparison of Clinical Performance of Two Monthly Replacement Toric Soft Contact Lenses | COMPLETED | NA | 2024-01-23 | 2024-05-12 | 2024-05-12 |
| NCT05769153 | Study of AR-14034 in Participants With Neovascular Age-Related Macular Degeneration (nAMD) | RECRUITING | PHASE1, PHASE2 | 2023-12-06 | 2027-09 | 2027-09 |
| NCT06071104 | Next Generation Cataract Surgery Study | COMPLETED | NA | 2023-12-06 | 2024-06-28 | 2024-05-23 |
| NCT05902364 | Systane® Ultra Preservative Free Lubricant Eye Drops | COMPLETED | NA | 2023-10-28 | 2024-08-14 | 2024-08-14 |
| NCT06021353 | Contralateral Study of WaveLight® Femtosecond Laser Devices for Corneal Flap Creation | COMPLETED | NA | 2023-10-20 | 2024-12-12 | 2024-12-12 |
| NCT06044948 | Clinical Assessment of a Daily Disposable Soft Silicone Hydrogel Contact Lens | COMPLETED | NA | 2023-10-13 | 2023-11-08 | 2023-11-08 |
| NCT05932238 | Systane® Hydration PF and Systane® Hydration Preserved | COMPLETED | NA | 2023-10-06 | 2024-09-05 | 2024-09-05 |
| NCT05796453 | Post Market Clinical Follow-up (PMCF) Study of Clareon Vivity & Clareon PanOptix | ACTIVE_NOT_RECRUITING | NA | 2023-09-19 | 2028-06 | 2028-06 |
| NCT05932225 | Systane® Complete Preservative Free Lubricant Eye Drops | COMPLETED | NA | 2023-08-18 | 2024-02-20 | 2024-02-20 |
| NCT05959200 | Clinical Performance Evaluation of Two Frequent Replacement Silicone Hydrogel Toric Contact Lenses | COMPLETED | NA | 2023-08-14 | 2023-10-23 | 2023-10-23 |
| NCT05888519 | Evaluation of Safety and Tolerability of Investigational Ocular Lubricants | COMPLETED | NA | 2023-07-24 | 2023-09-27 | 2023-09-27 |
| NCT05886907 | Assessing the Clinical Performance of Two Frequent Replacement Silicone Hydrogel Multifocal Toric Contact Lenses | COMPLETED | NA | 2023-06-14 | 2023-07-17 | 2023-07-17 |
| NCT05725317 | Clinical Performance Assessment of Two Silicone Hydrogel Daily Disposable Contact Lenses | COMPLETED | NA | 2023-06-02 | 2023-06-27 | 2023-06-27 |
| NCT05852470 | Evaluation of Clareon Vivity/Vivity Toric | COMPLETED | NA | 2023-05-23 | 2023-10-27 | 2023-10-27 |
| NCT05741216 | Evaluation of Comfort of Ocular Lubricants in Symptomatic Contact Lens Wearers | COMPLETED | NA | 2023-05-01 | 2023-10-02 | 2023-10-02 |
| NCT05805345 | Clinical Comparison of Toric Contact Lenses Fit Characteristics | WITHDRAWN | NA | 2023-04 | 2023-05 | 2023-05 |
| NCT05317728 | Clinical Study of a Fluid Accommodating Intraocular Lens (IOL) Design | RECRUITING | NA | 2023-03-31 | 2026-12 | 2026-12 |
| NCT05766787 | The Clinical Performance of Two Reusable Silicone Hydrogel Contact Lenses | COMPLETED | NA | 2023-03-29 | 2023-06-02 | 2023-06-02 |
| NCT05765227 | Clinical Evaluation of a Manufacturing Process for a Frequent Replacement Silicone Hydrogel Multifocal Contact Lens | COMPLETED | NA | 2023-03-08 | 2023-03-30 | 2023-03-30 |
| NCT05702541 | Assessing the Clinical Performance of Two Frequent Replacement Silicone Hydrogel Multifocal Contact Lenses | COMPLETED | NA | 2023-01-24 | 2023-02-21 | 2023-02-21 |
| NCT05573360 | Evaluation of Safety and Tolerability of Ocular Lubricants | COMPLETED | NA | 2022-12-16 | 2023-05-31 | 2023-05-31 |
| NCT05481125 | Clareon Toric vs Eyhance Toric | COMPLETED | NA | 2022-10-10 | 2023-10-16 | 2023-10-16 |
| NCT05483127 | Clinical Comparison of Two Daily Disposable Toric Soft Contact Lenses | COMPLETED | NA | 2022-09-13 | 2022-10-31 | 2022-10-31 |
| NCT05431478 | Clinical Performance of Two Reusable Silicone Hydrogel Contact Lenses | COMPLETED | NA | 2022-07-15 | 2022-09-09 | 2022-09-09 |
| NCT05338333 | Clinical Performance Evaluation of Two Frequent Replacement Silicone Hydrogel Multifocal Contact Lenses | COMPLETED | NA | 2022-05-27 | 2022-09-01 | 2022-09-01 |
| NCT05211739 | Clinical Assessment of a Daily Wear Monthly Replacement Silicone Hydrogel Toric Contact Lens | COMPLETED | NA | 2022-02-15 | 2022-06-23 | 2022-06-23 |
| NCT05056233 | Systane Hydration in Subjects Undergoing Cataract Surgery | COMPLETED | NA | 2022-01-18 | 2023-01-12 | 2023-01-12 |
| NCT05056987 | Clinical Assessment of Two Daily Wear Reusable Soft Silicone Hydrogel Contact Lenses | COMPLETED | NA | 2022-01-12 | 2022-06-14 | 2022-06-14 |
| NCT05138783 | Clinical Performance of Two Daily Disposable Soft Contact Lenses | COMPLETED | NA | 2022-01-12 | 2022-03-07 | 2022-03-07 |
| NCT05198297 | Safety and Effectiveness of the Hydrus Microstent | TERMINATED | NA | 2021-12-13 | 2024-01-31 | 2024-01-31 |
| NCT05056155 | Systane Complete Multi-symptom Relief | COMPLETED | NA | 2021-11-09 | 2022-03-25 | 2022-03-25 |
| NCT05050578 | Clinical Assessment of Two Reusable Silicone Hydrogel Contact Lenses | COMPLETED | NA | 2021-11-02 | 2022-02-22 | 2022-02-22 |
| NCT05039112 | Clinical Comparison of 2 Daily Disposable Toric Soft Contact Lenses | COMPLETED | NA | 2021-09-28 | 2021-11-29 | 2021-11-29 |
| NCT05010512 | Clinical Performance of Two Commercial, Daily Disposable Contact Lenses | COMPLETED | NA | 2021-08-31 | 2021-10-12 | 2021-10-12 |
| NCT04980456 | Clinical Assessment of Two Daily Wear Monthly Replacement Soft Silicone Hydrogel Contact Lenses | COMPLETED | NA | 2021-08-05 | 2021-11-20 | 2021-11-20 |
| NCT04963543 | Evaluation of Comfort in Symptomatic Contact Lens Wearers | COMPLETED | NA | 2021-07-22 | 2021-10-29 | 2021-10-29 |
| NCT04942925 | Clinical Comparison of Two Daily Disposable Contact Lenses - Pilot Study 3 | COMPLETED | NA | 2021-07-20 | 2021-09-09 | 2021-09-09 |
| NCT04908488 | Clinical Performance of Two Daily Disposable Toric Soft Contact Lenses | COMPLETED | NA | 2021-07-01 | 2021-09-22 | 2021-09-22 |
| NCT04830956 | Evaluation of Comfort in Subjects With Moderate Dry Eye Disease | COMPLETED | NA | 2021-06-30 | 2021-11-10 | 2021-11-10 |
| NCT04800016 | Real-World Study of Vivity Intraocular Lenses (IOLs) | WITHDRAWN | NA | 2021-06 | 2024-07 | 2024-01 |
| NCT04865354 | Clinical Comparison of Two Daily Disposable Contact Lenses | COMPLETED | NA | 2021-05-17 | 2021-06-27 | 2021-06-27 |
| NCT04805593 | Clinical Investigation of the WaveLight® EX500 Excimer Laser | COMPLETED | NA | 2021-04-28 | 2023-05-02 | 2023-05-02 |
| NCT04755231 | Post-Market Clinical Study of the PanOptix Intraocular Lens (IOL) in a Chinese Population | COMPLETED | NA | 2021-04-19 | 2023-03-15 | 2022-08-31 |
| NCT04789382 | Three Daily Wear Monthly Replacement Silicone Hydrogel Contact Lenses With Two Multi-purpose Disinfecting Solution Combinations | COMPLETED | NA | 2021-04-07 | 2021-05-07 | 2021-05-07 |
| NCT04702984 | Clinical Characterization of an Investigational Frequent Replacement Daily Wear Silicone Hydrogel Sphere Contact Lens | COMPLETED | NA | 2021-01-21 | 2021-02-26 | 2021-02-26 |
| NCT04330001 | Exploratory Clinical Study for Techniques Associated With the Fluid Accommodating IOL | COMPLETED | NA | 2020-12-28 | 2023-05-03 | 2022-06-08 |
| NCT04629521 | Additional Long-Term Follow-up for Subjects Implanted With a CyPass® Micro-Stent | COMPLETED | NA | 2020-12-21 | 2023-04-05 | 2023-04-05 |
| NCT04631796 | Clinical Characterization of an Investigational Soft Silicone Hydrogel Contact Lens | COMPLETED | NA | 2020-12-03 | 2020-12-31 | 2020-12-31 |
| NCT04542525 | Clinical Investigation of an AcrySof IQ PanOptix Toric Intraocular Lens | COMPLETED | NA | 2020-12-01 | 2021-08-10 | 2021-08-10 |
| NCT04528069 | Clinical Investigation of the Visual Outcomes and Safety of a Trifocal Toric IOL in an Asian Population | COMPLETED | NA | 2020-11-16 | 2021-12-17 | 2021-12-17 |
| NCT04422990 | Clinical Evaluation of a Silicone Hydrogel Daily Wear Monthly Replacement Contact Lens | COMPLETED | NA | 2020-10-01 | 2021-05-18 | 2021-02-22 |
| NCT04527978 | Clinical Comparison of 2 Daily Disposable Contact Lenses - Pilot Study 1 | COMPLETED | NA | 2020-09-15 | 2020-11-06 | 2020-11-06 |
| NCT04532099 | Clinical Comparison of Two Daily Wear Frequent Replacement Silicone Hydrogel Soft Contact Lenses | COMPLETED | NA | 2020-09-09 | 2021-05-04 | 2021-05-04 |
| NCT04528017 | Clinical Comparison of 2 Daily Disposable Contact Lenses - Pilot Study 2 | COMPLETED | NA | 2020-09-01 | 2020-10-16 | 2020-10-16 |
| NCT04553523 | Hydrus® Microstent New Enrollment Post-Approval Study | RECRUITING | NA | 2020-08-25 | 2028-06 | 2028-06 |
| NCT04476784 | Clinical Assessment of a Daily Wear Monthly Replacement Soft Silicone Hydrogel Contact Lens | COMPLETED | NA | 2020-08-17 | 2020-11-18 | 2020-11-18 |
| NCT04403542 | Pilot Clinical Performance of a Silicone Hydrogel Lens for Up to Six Nights of Extended Wear | COMPLETED | NA | 2020-08-03 | 2020-08-31 | 2020-08-31 |
| NCT04464044 | Clinical Performance of a Daily Disposable Toric Silicone Hydrogel Contact Lens | COMPLETED | NA | 2020-07-20 | 2020-08-06 | 2020-08-06 |
| NCT04219891 | WaveLight® EX500 Excimer Laser System for the Correction of Myopia Using InnovEyes™ in Conjunction With InnovEyes™ Sightmap | COMPLETED | NA | 2020-03-09 | 2022-11-09 | 2022-11-09 |
| NCT04254003 | Clinical Performance Evaluation of Two Daily Disposable Silicone Hydrogel Toric Contact Lenses | COMPLETED | NA | 2020-02-05 | 2020-03-02 | 2020-03-02 |
| NCT04178720 | Clinical Evaluation of a Daily Wear Monthly Replacement Silicone Hydrogel Lens | COMPLETED | NA | 2020-01-28 | 2020-06-10 | 2020-06-10 |
| NCT04207749 | Clinical Evaluation of a Daily Wear Silicone Hydrogel Lens | COMPLETED | NA | 2020-01-22 | 2020-12-17 | 2020-12-17 |
| NCT04098367 | Clinical Investigation of the AcrySof IQ Vivity Extended Vision Intraocular Lens (IOL) | COMPLETED | NA | 2019-11-18 | 2021-07-22 | 2021-05-03 |
| NCT04085328 | Assessment of an Investigational Frequent Replacement Silicone Hydrogel Lens | COMPLETED | NA | 2019-10-11 | 2021-03-26 | 2021-03-26 |
| NCT04055519 | Clinical Performance Assessment of a Daily Wear Monthly Replacement Soft Silicone Hydrogel Contact Lens | COMPLETED | NA | 2019-09-19 | 2019-12-03 | 2019-12-03 |
| NCT04013789 | Comparison of Two Daily Disposable Lenses | COMPLETED | NA | 2019-08-27 | 2019-11-22 | 2019-11-22 |
| NCT03956225 | Comparison Between iLux and LipiFlow in the Treatment of Meibomian Gland Dysfunction (MGD): A 12-month, Multicenter Study | COMPLETED | NA | 2019-06-25 | 2020-10-24 | 2020-10-24 |
| NCT03969290 | Clinical Performance of Two Daily Disposable Contact Lenses - Study 1 | COMPLETED | NA | 2019-06-05 | 2019-08-05 | 2019-08-05 |
| NCT03920280 | Clinical Evaluation of a Daily Wear Frequent Replacement Silicone Hydrogel Lens | COMPLETED | NA | 2019-05-22 | 2019-10-05 | 2019-10-05 |
| NCT03888469 | Clinical Comparison of DDT2 Contact Lens and a Daily Disposable Contact Lens - Study 1 | COMPLETED | NA | 2019-05-03 | 2019-06-24 | 2019-06-24 |
| NCT03888482 | Clinical Comparison of DDT2 Contact Lens and a Daily Disposable Contact Lens - Study 2 | COMPLETED | NA | 2019-04-26 | 2019-06-28 | 2019-06-28 |
| NCT03757039 | Multifocal Visual Performance Study | TERMINATED | NA | 2018-12-16 | 2019-03-06 | 2019-03-06 |
| NCT03762668 | Performance Assessment of a Modified Daily Disposable Contact Lens | COMPLETED | NA | 2018-12-03 | 2019-01-07 | 2019-01-07 |
| NCT03733730 | Post Approval Study of the AcrySof® IQ ReSTOR® Toric IOLs | COMPLETED | NA | 2018-11-27 | 2022-10-14 | 2022-10-14 |
| NCT03614130 | Clinical Performance of a Silicone Hydrogel Contact Lens Following Six Nights of Extended Wear | COMPLETED | NA | 2018-08-23 | 2018-09-11 | 2018-09-11 |
| NCT03479944 | Clinical Evaluation of FLACS With Combination of LenSx® and Centurion® | COMPLETED | NA | 2018-08-22 | 2019-05-17 | 2018-11-19 |
| NCT03579433 | Postmarket Study of an Intraocular Lens Power Selection System | COMPLETED | NA | 2018-08-16 | 2019-04-16 | 2019-04-16 |
| NCT03628599 | Two Daily Disposable Contact Lenses in Symptomatic Patients | COMPLETED | NA | 2018-08-13 | 2018-09-25 | 2018-09-25 |
| NCT03586167 | Clinical Performance of a Monthly Replacement Silicone Hydrogel Lens | COMPLETED | NA | 2018-08-01 | 2018-09-27 | 2018-09-27 |
| NCT03492541 | Study of Efficacy and Tolerability of SYSTANE Complete in Patients With Dry Eye Disease | COMPLETED | NA | 2018-07-18 | 2019-05-14 | 2019-04-30 |
| NCT03560141 | Clinical Performance of a Silicone Hydrogel Contact Lens Following One Night of Extended Wear | COMPLETED | NA | 2018-07-11 | 2018-07-17 | 2018-07-17 |
| NCT03567005 | Clinical Validation of DACP Digital Design | COMPLETED | NA | 2018-06-25 | 2018-08-26 | 2018-08-26 |
| NCT03518008 | Clinical Comparison of Two Daily Disposable Soft Contact Lenses | COMPLETED | NA | 2018-05-23 | 2018-06-11 | 2018-06-11 |
| NCT03316885 | Post-Market Clinical Investigation of the Clareon® IOL | COMPLETED | NA | 2018-03-14 | 2021-09-23 | 2019-10-18 |
| NCT03459131 | Clinical Evaluation of Two Monthly Contact Lenses | COMPLETED | NA | 2018-03-07 | 2018-03-26 | 2018-03-26 |
| NCT03350503 | AcrySof IQ Toric A-Code Post-Market Clinical Study | COMPLETED | NA | 2018-01-30 | 2021-12-17 | 2019-05-23 |
| NCT03349632 | Clinical Comparison of 4 Daily Disposable Soft Contact Lenses | COMPLETED | NA | 2018-01-10 | 2018-02-16 | 2018-02-16 |
| NCT03268746 | Clinical Investigation of the Visual Outcomes and Safety of a Trifocal Intraocular Lens (IOL) in a Korean Population | COMPLETED | NA | 2018-01-09 | 2018-11-30 | 2018-11-30 |
| NCT03392532 | Comparison of Two Silicone Hydrogel Toric Contact Lenses | COMPLETED | NA | 2018-01-04 | 2018-01-26 | 2018-01-26 |
| NCT03341923 | Clinical Evaluation of DAILIES TOTAL 1® Multifocal Compared to 1-Day Acuvue® Moist® Multifocal in a Japanese Population | COMPLETED | NA | 2017-12-20 | 2018-06-05 | 2018-06-05 |
| NCT03280108 | Clinical Investigation of AcrySof® IQ PanOptix™ IOL Model TFNT00 | COMPLETED | NA | 2017-11-01 | 2018-09-27 | 2018-09-27 |
| NCT03273907 | Post Approval Study of the CyPass System | TERMINATED | NA | 2017-10-12 | 2021-08-31 | 2021-08-31 |
| NCT03305770 | DD T2 Daily Disposable Registration Trial | COMPLETED | NA | 2017-10-12 | 2018-02-21 | 2018-02-21 |
| NCT03274986 | A Clinical Study of the ACRYSOF® IQ Extended Depth of Focus Intraocular Lens (IOL) | COMPLETED | NA | 2017-10-11 | 2018-10-16 | 2018-10-16 |
| NCT03169153 | Clinical Comparison of Silicone Hydrogel Monthly Lenses | COMPLETED | NA | 2017-09-22 | 2018-07-19 | 2018-07-19 |
| NCT03170154 | Clinical Investigation of the Clareon® Intraocular Lens (IOL) | COMPLETED | NA | 2017-07-25 | 2019-02-15 | 2019-02-15 |
| NCT03118934 | Assessing Fitting Guides in Alcon Multifocal Contact Lenses | COMPLETED | NA | 2017-05-17 | 2017-07-28 | 2017-07-07 |
| NCT03095027 | Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear | COMPLETED | NA | 2017-04-19 | 2017-05-15 | 2017-05-15 |
| NCT03090256 | Clinical Investigation of the AcrySof® IQ PanOptix™ IOL | COMPLETED | NA | 2017-04-11 | 2018-02-13 | 2018-02-13 |
| NCT03010254 | A Clinical Study of the ACRYSOF® IQ EDF Intraocular Lens (IOL) | COMPLETED | NA | 2017-03-21 | 2018-10-31 | 2018-08-17 |
| NCT03021707 | Early Feasibility Study of UV-Femtosecond Laser Assisted Lenticular Extraction | COMPLETED | NA | 2017-03-07 | 2019-10-17 | 2019-05-27 |
| NCT02987660 | Comparison of Topography Guided LASIK With WaveLight® EX500 to SMILE With Zeiss VisuMax | TERMINATED | NA | 2017-03-03 | 2017-07-26 | 2017-07-26 |
| NCT02974140 | Cataract Refractive Suite Study | TERMINATED | NA | 2017-03-02 | 2017-07-25 | 2017-07-25 |
| NCT03034928 | Clinical Biocompatibility Evaluation of Contact Lens Coatings | COMPLETED | NA | 2017-02-14 | 2017-03-14 | 2017-03-14 |
| NCT03026257 | Clinical Assessment of a HYDRAGLYDE® Regimen | COMPLETED | NA | 2017-02-13 | 2017-08-18 | 2017-08-18 |
| NCT02965820 | OPTI-FREE® PureMoist® for Presbyopic Contact Lens Wearers | COMPLETED | NA | 2016-12-16 | 2017-04-01 | 2017-04-01 |
| NCT02965833 | CLEAR CARE® PLUS for Presbyopic Contact Lens Wearers | COMPLETED | NA | 2016-12-13 | 2017-03-24 | 2017-03-24 |
| NCT02939170 | Initial Performance of a Daily Disposable Contact Lens Featuring Molded Marks | COMPLETED | NA | 2016-11-14 | 2016-12-02 | 2016-12-02 |
| NCT02842151 | Optimizing the Assessment of Refractive Outcomes After Cataract Surgery | COMPLETED | NA | 2016-09-21 | 2017-11-16 | 2017-11-16 |
| NCT02871375 | Clinical Assessment of DAILIES TOTAL1® (DT1) Multifocal | COMPLETED | NA | 2016-08-30 | 2016-11-14 | 2016-11-14 |
| NCT02776670 | Clinical Outcomes Following Treatment With SYSTANE® BALANCE | COMPLETED | NA | 2016-07-29 | 2017-11-22 | 2017-11-22 |
| NCT02826421 | Clinical Investigation of Corneal Incision Size After Intraocular Lens (IOL) Implantation | COMPLETED | NA | 2016-07-04 | 2016-11-29 | 2016-11-29 |
| NCT02730871 | Safety and Efficacy of SIMBRINZA® BID as an Adjunctive to DUOTRAV® | TERMINATED | PHASE4 | 2016-06-24 | 2018-07-13 | 2018-07-13 |
| NCT02770248 | 24-hr Intraocular Pressure Control With SIMBRINZA ® | COMPLETED | PHASE4 | 2016-05-23 | 2017-01-14 | 2017-01-14 |
| NCT02771145 | Clinical Evaluation of the Safety and Efficacy of FID 120947A | COMPLETED | NA | 2016-05-20 | 2017-01-10 | 2017-01-10 |
| NCT02699684 | Comparison of Lotrafilcon B Lenses With Different Packaging Solutions | COMPLETED | NA | 2016-05-12 | 2016-10-20 | 2016-10-20 |
| NCT02691741 | Clinical Investigation of Visual Function After Bilateral Implantation of Two Presbyopia-Correcting Trifocal Intraocular Lenses (IOL) | COMPLETED | NA | 2016-04-29 | 2017-07-17 | 2017-07-17 |
| NCT02750813 | ACUVUE® OASYS® 1-DAY vs DAILIES TOTAL1® | COMPLETED | NA | 2016-04-27 | 2016-08-17 | 2016-08-17 |
| NCT02710292 | Clinical Evaluation of DAILIES TOTAL 1® Performance in a Japanese Population | COMPLETED | NA | 2016-04-25 | 2016-09-14 | 2016-09-14 |
| NCT02700984 | A Study to Assess Long-Term Safety of the CyPass Micro-Stent in Patients Completing the COMPASS Trial | COMPLETED | NA | 2016-03-30 | 2018-04-18 | 2018-04-18 |
| NCT02694835 | Initial Performance of a Modified Daily Disposable Contact Lens | COMPLETED | NA | 2016-03-21 | 2016-04-11 | 2016-04-11 |
| NCT02696317 | Clinical Evaluation of ACUVUE® OASYS® 1-Day and ACUVUE® OASYS® | COMPLETED | NA | 2016-03-18 | 2016-06-06 | 2016-06-06 |
| NCT02743780 | A Three Part Study of MGV354 in Ocular Hypertension or Glaucoma | COMPLETED | PHASE1, PHASE2 | 2016-03-02 | 2016-09-20 | 2016-09-20 |
| NCT02281292 | A Study of the Safety and Tolerability of Intravitreal LKA651 in Patients With Diabetic Macular Edema | WITHDRAWN | PHASE1 | 2015-12 | 2017-06 | 2017-06 |
| NCT02511379 | Clinical Evaluation of Systane® Balance in Dry Eye Subjects | TERMINATED | NA | 2015-11-26 | 2016-06-20 | 2016-06-20 |
| NCT02539654 | Pediatric Pharmacokinetic (PK) Study of EXE844 Otic Suspension in Otitis Media at the Time of Tympanostomy Tube Insertion (OMTT) | COMPLETED | PHASE1 | 2015-11-17 | 2016-06-24 | 2016-06-24 |
| NCT02575911 | Accuracy of LASIK Flaps Created With the LenSx® Femtosecond Laser - A Pilot Study | COMPLETED | NA | 2015-10-28 | 2016-04-09 | 2016-04-09 |
| NCT02515942 | CLG561 Proof-of-Concept Study as a Monotherapy and in Combination With LFG316 in Subjects With Geographic Atrophy (GA) | COMPLETED | PHASE2 | 2015-09-25 | 2017-12-01 | 2017-08-14 |
| NCT02517567 | DAILIES TOTAL1® - Comparative Assessment of Tear Film Evaporation | COMPLETED | NA | 2015-09-21 | 2016-04-22 | 2016-04-22 |
| NCT02529488 | Investigation of AcrySof® IQ PanOptix™ Presbyopia-Correcting Intraocular Lens (IOL) Model TFNT00 | COMPLETED | NA | 2015-09-07 | 2017-06-26 | 2016-11-30 |
| NCT02380261 | A Clinical Study of Systane® Lid Wipes in Brazil | COMPLETED | NA | 2015-09 | 2015-10 | 2015-10 |
| NCT02507388 | Safety and Pharmacokinetics of RTH258 in Subjects With Age-Related Macular Degeneration | COMPLETED | PHASE2 | 2015-08-24 | 2016-09-06 | 2016-09-06 |
| NCT02419508 | SIMBRINZA® Suspension BID as an Adjunctive to Prostaglandin Analogue (PGA) | COMPLETED | PHASE4 | 2015-08-07 | 2018-02-27 | 2018-02-27 |
| NCT02434328 | Efficacy and Safety of RTH258 Versus Aflibercept - Study 2 | COMPLETED | PHASE3 | 2015-07-28 | 2018-03-08 | 2017-04-05 |
| NCT02502526 | Comparison of Centurion® Vision System With Balanced Tip and the Infiniti® Vision System With the Mini Flared Kelman (MFK) Tip During Cataract Extraction Surgery of Hard Lenses | COMPLETED | NA | 2015-07-27 | 2017-11-30 | 2017-03-23 |
| NCT02398500 | Safety Tolerability and Efficacy of Intravitreal LMG324 in the Treatment of Neovascular Age-Related Macular Degeneration | TERMINATED | PHASE1, PHASE2 | 2015-07-22 | 2016-05-20 | 2016-02-29 |
| NCT02482129 | Proof of Concept Study to Evaluate Safety and Efficacy of LME636 in the Treatment of Acute Anterior Uveitis | COMPLETED | PHASE2 | 2015-07-17 | 2016-03-21 | 2016-03-21 |
| NCT02470429 | Evaluation of Clinical Outcomes After the Use of SYSTANE® HYDRATION | COMPLETED | NA | 2015-07-17 | 2016-05-26 | 2016-05-26 |
| NCT02477605 | Clinical Comparison of 27+® and 23-gauge ULTRAVIT® 7500 Cpm Vitrectomy Outcomes | COMPLETED | NA | 2015-07-16 | 2016-08-31 | 2016-06-01 |
| NCT02495948 | Comparison of Two Marketed Silicone Hydrogel Lenses | COMPLETED | NA | 2015-07 | 2015-10 | 2015-10 |
| NCT02432105 | Safety and Efficacy of EXE844 Otic Suspension in Otitis Media at Time of Tympanostomy Tube Insertion (OMTT) | COMPLETED | PHASE3 | 2015-06-25 | 2016-06-15 | 2016-06-15 |
| NCT02436304 | Safety and Efficacy of EXE844 Otic Suspension in Otitis Media at Time of Tympanostomy Tube Insertion (OMTT) - Study 2 | COMPLETED | PHASE3 | 2015-06-19 | 2016-08-04 | 2016-08-04 |
| NCT02446015 | Clinical Evaluation Following Use of SYSTANE® ULTRA in the Management of Dry Eye | COMPLETED | NA | 2015-06-19 | 2016-06-21 | 2016-06-21 |
| NCT02450799 | Corrected VA With Long-Term Follow-Up After AcrySof® Intraocular Lens (IOL) Implantation | COMPLETED | NA | 2015-06 | 2016-05 | 2016-05 |
| NCT02322229 | Ocriplasmin for Vitreomacular Traction/Symptomatic Vitreomacular Adhesion | COMPLETED | PHASE4 | 2015-05-26 | 2016-05-09 | 2015-12-11 |
| NCT02380248 | Clinical Evaluation of Systane® Gel Drops in Dry Eye Subjects | COMPLETED | NA | 2015-05-14 | 2016-06-01 | 2016-06-01 |
| NCT02403180 | DAILIES® AquaComfort Plus® Multifocal (MF) - Comparative Assessment of Visual Performance | COMPLETED | NA | 2015-05 | 2015-07 | 2015-07 |
| NCT02402127 | Lubricity Post-Wear - Competitive Lenses Pilot | COMPLETED | NA | 2015-05 | 2015-07 | 2015-07 |
| NCT02339584 | Efficacy and Safety of Brinzolamide/Brimonidine Fixed Combination BID Compared to Brinzolamide BID Plus Brimonidine BID in Subjects With Open-Angle Glaucoma (OAG) or Ocular Hypertension (OHT) | COMPLETED | PHASE3 | 2015-04-14 | 2016-11-01 | 2016-11-01 |
| NCT02388763 | Clinical Evaluation of MyDay™ and 1-DAY ACUVUE® TruEye® | COMPLETED | NA | 2015-04 | 2015-09 | 2015-09 |
| NCT02413333 | Clear Care® Plus vs. PeroxiClear™ | COMPLETED | NA | 2015-04 | 2015-08 | 2015-08 |
| NCT02403206 | Femtosecond Laser Assisted Cataract Surgery in Intumescent Cataracts | COMPLETED | NA | 2015-03-26 | 2016-08-24 | 2016-07-12 |
| NCT02365519 | LME636 in the Relief of Persistent Ocular Discomfort in Subjects With Severe Dry Eye Disease | COMPLETED | PHASE2 | 2015-03-09 | 2015-10-16 | 2015-10-16 |
| NCT02355028 | LHA510 Proof-of-Concept Study as a Maintenance Therapy for Patients With Wet Age-Related Macular Degeneration | COMPLETED | PHASE2 | 2015-03-03 | 2016-10-18 | 2016-09-15 |
| NCT02307682 | Efficacy and Safety of RTH258 Versus Aflibercept - Study 1 | COMPLETED | PHASE3 | 2014-12-08 | 2018-03-28 | 2017-04-22 |
| NCT02322216 | Olopatadine Hydrochloride Ophthalmic Solution Study in Chinese Subjects | COMPLETED | PHASE3 | 2014-12 | 2015-10 | 2015-10 |
| NCT02325518 | Comparison of Intraocular Pressure (IOP)-Lowering Efficacy and Safety of AZORGA® Ophthalmic Suspension and COSOPT® Ophthalmic Solution | COMPLETED | PHASE4 | 2014-12 | 2015-12 | 2015-12 |
| NCT02289742 | Tear Film Evaluation of Dailies® AquaComfort Plus® Multifocal and Toric | COMPLETED | NA | 2014-12 | 2015-03 | 2015-03 |
| NCT02293538 | Formula Identification (FID) 114657 in Contact Lens Wearers | COMPLETED | NA | 2014-11 | 2015-07 | 2015-07 |
| NCT01908764 | Pharmacokinetic Study of AL-60371 Otic Suspension in Pediatric Subjects Following Tympanostomy Tube Surgery | WITHDRAWN | PHASE1 | 2014-11 | 2015-01 | 2015-01 |
| NCT02219997 | Functional Vision With ACRYSOF® IQ IOLs Blue Light Filtration | COMPLETED | NA | 2014-10 | 2015-03 | 2015-03 |
| NCT02252133 | DAILIES TOTAL1® Lens Centration in a Japanese Population | COMPLETED | NA | 2014-10 | 2014-11 | 2014-11 |
| NCT02235831 | DAILIES® AquaComfort Plus® Multifocal (MF) - Comparative Assessment of Visual Performance | COMPLETED | NA | 2014-09 | 2014-10 | 2014-10 |
| NCT02189863 | Driving Simulator Study Comparing Two Modes of Presbyopic Correction With Contact Lenses | COMPLETED | NA | 2014-08 | 2014-12 | 2014-12 |
| NCT02176343 | Retrospective / Prospective Clinical Study of AcrySof® IQ ReSTOR® +2.5 D Multifocal Toric Intraocular Lenses | COMPLETED | NA | 2014-07-21 | 2014-08-22 | 2014-08-22 |
| NCT02140060 | 6-Week Proof-of-Concept Study of Travoprost/Brinzolamide Ophthalmic Suspension in Subjects With Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE2 | 2014-06 | 2014-11 | 2014-11 |
| NCT02175199 | A Comparison of Two Color Contact Lenses in Habitual Clear Contact Lens Wearers | COMPLETED | NA | 2014-06 | 2014-09 | 2014-09 |
| NCT02157909 | DW Evaluation of Lotrafilcon B Lenses in a Modified Design | COMPLETED | NA | 2014-06 | 2014-07 | 2014-07 |
| NCT02035748 | Assessment of Patients Treated With JETREA® for Vitreomacular Traction | COMPLETED | PHASE4 | 2014-04 | 2015-09 | 2015-09 |
| NCT02071771 | Visual Assessment of DAILIES® AquaComfort Plus® for Astigmatism as Compared to 1-DAY ACUVUE® MOIST® for Astigmatism | COMPLETED | NA | 2014-04 | 2014-09 | 2014-09 |
| NCT02117544 | Multifocal High ADD Contact Lens Proof of Concept Trial | COMPLETED | NA | 2014-04 | 2014-07 | 2014-07 |
| NCT02079649 | Safety and Efficacy Study of AL-53817 and AL-78843 Ophthalmic Solutions for Allergic Conjunctivitis | COMPLETED | PHASE2 | 2014-04 | 2014-07 | 2014-07 |
| NCT02066922 | A Comparative Study of Two Daily Disposable Contact Lenses in Higher Myopia Subjects | COMPLETED | NA | 2014-03 | 2014-05 | 2014-05 |
| NCT02089191 | Tear Film Stability of DAILIES® AquaComfort Plus® Contact Lenses vs. MyDay® Daily Disposable Contact Lenses | COMPLETED | NA | 2014-03 | 2014-04 | 2014-04 |
| NCT02072980 | DAILIES TOTAL1® Lubricity Post Wear | COMPLETED | NA | 2014-03 | 2014-04 | 2014-04 |
| NCT01515826 | VIGADEXA Gel Compared to VIGADEXA Solution Following Cataract Surgery | WITHDRAWN | PHASE3 | 2014-03 | 2014-10 | 2014-10 |
| NCT02246777 | Alcon® Ex-PRESS® Glaucoma Filtration Device in Japanese Patients | COMPLETED | NA | 2014-02-26 | 2016-10-24 | 2016-10-24 |
| NCT02076919 | First-in-Human Study of LHA510 in Elderly Subjects and Patients With Age-Related Macular Degeneration | COMPLETED | PHASE1 | 2014-02 | 2014-06 | 2014-06 |
| NCT01967147 | Clinical Outcomes Following Treatment With Systane® Balance in Dry Eye Subjects | COMPLETED | NA | 2014-02 | 2015-01 | 2015-01 |
| NCT01908803 | Proof-of-Concept Study of a Single Application of an Investigational Otic Suspension in Treatment of Acute Otitis Media With Tympanostomy Tubes | TERMINATED | PHASE2 | 2013-12 | 2014-08 | 2014-08 |
| NCT02003391 | Efficacy of Travoprost/Timolol for Uncontrolled Intraocular Pressure | COMPLETED | PHASE4 | 2013-12 | 2015-05 | 2015-05 |
| NCT02251613 | Effectiveness of Olopatadine HCl Ophthalmic Solution for the Treatment of Allergic Conjunctivitis in Japan | COMPLETED | PHASE4 | 2013-12 | 2014-01 | 2014-01 |
| NCT01912768 | Safety and Efficacy Evaluation of a New Contact Lens Disinfecting Solution in Soft Contact Lens Wearers | COMPLETED | NA | 2013-12 | 2014-05 | 2014-05 |
| NCT01996709 | Effectiveness of a Marketed One-Step Peroxide Lens Care Solution in Symptomatic Contact Lens Wearers | COMPLETED | NA | 2013-12 | 2014-05 | 2014-05 |
| NCT02251561 | Clinical Evaluation of Opti-Free III (FID 109182) Compared to Opti-Free Plus® in Japan | COMPLETED | NA | 2013-11 | 2014-05 | 2014-05 |
| NCT01912781 | Safety and Efficacy Evaluation of a New Contact Lens Disinfecting Solution in Gas Permeable Contact Lens Wearers | COMPLETED | NA | 2013-11 | 2014-05 | 2014-05 |
| NCT01941485 | WaveLight® Refractive Flap Accuracy Study | COMPLETED | NA | 2013-10 | 2015-02 | 2014-01 |
| NCT01937312 | Effect of SIMBRINZA® Suspension as an Added Therapy to a Prostaglandin Analogue | COMPLETED | PHASE4 | 2013-10 | 2014-05 | 2014-05 |
| NCT01937299 | Effect of SIMBRINZA® Suspension as an Added Therapy to TRAVATAN Z® | COMPLETED | PHASE4 | 2013-10 | 2014-04 | 2014-04 |
| NCT01978600 | Evaluation of Intraocular Pressure Using Simbrinza™ in Patients With Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE4 | 2013-10 | 2014-03 | 2014-03 |
| NCT01951573 | Evaluation of a New Daily Disposable Multifocal Contact Lens Design | COMPLETED | NA | 2013-10 | 2013-11 | 2013-11 |
| NCT02103309 | Comparative Evaluation of Contact Lens Centering of DAILIES® AquaComfort Plus® Versus 1-DAY ACUVUE® MOIST® in Japan | COMPLETED | NA | 2013-10 | 2013-11 | 2013-11 |
| NCT01941498 | WaveLight® Refractive Myopic Study | COMPLETED | NA | 2013-09 | 2014-08 | 2014-01 |
| NCT01995136 | Investigation of Intraocular Pressure (IOP) Reduction Efficacy of Travoprost Ophthalmic Solution in Patients With Normal Tension Glaucoma | COMPLETED | PHASE4 | 2013-09 | 2014-06 | 2014-06 |
| NCT01863368 | Clinical Evaluation of Systane® ULTRA Compared to OPTIVE® in Ocular Surface Staining | COMPLETED | NA | 2013-09 | 2014-06 | 2014-06 |
| NCT01938989 | Effect of Blue Light Filtration on Visual Performance | COMPLETED | NA | 2013-09 | 2014-01 | 2014-01 |
| NCT01917162 | Multi-Center Clinical Evaluation of Two Daily Disposable Contact Lenses (Study 2) | COMPLETED | NA | 2013-09 | 2013-11 | 2013-11 |
| NCT01898260 | Multi-Center Clinical Evaluation of Two Daily Disposable Contact Lenses | COMPLETED | NA | 2013-08 | 2013-10 | 2013-10 |
| NCT01889251 | A Phase III Study of A01016 in Subjects With Symptomatic Vitreomacular Adhesion | COMPLETED | PHASE3 | 2013-07 | 2014-09 | 2014-09 |
| NCT01848288 | Intra-Operative Metrics With CENTURION® and INFINITI® Vision Systems | COMPLETED | NA | 2013-07 | 2014-02 | 2014-02 |
| NCT01870856 | Lid Wiper Epitheliopathy Trial | TERMINATED | NA | 2013-07 | 2013-10 | 2013-10 |
| NCT01629693 | Clinical Evaluation of Two Monthly Replacement Silicone Hydrogel Contact Lenses | COMPLETED | NA | 2013-07 | 2013-11 | 2013-11 |
| NCT02448875 | Clinical Evaluation of Visco-Assisted CyPass® Micro-Stent Implantation in Patients With Open Angle Glaucoma | COMPLETED | NA | 2013-06-21 | 2017-06-22 | 2017-06-22 |
| NCT01853072 | Nepafenac Once Daily for Macular Edema - Study 1 | COMPLETED | PHASE3 | 2013-06 | 2015-05 | 2015-05 |
| NCT01872611 | Nepafenac Once Daily for Macular Edema - Study 2 | COMPLETED | PHASE3 | 2013-06 | 2015-05 | 2015-05 |
| NCT01849692 | ESBA1008 Microvolume Study | COMPLETED | PHASE2 | 2013-06 | 2015-01 | 2015-01 |
| NCT01835015 | Pharmacokinetics of CLG561 in Patients With Advanced Age-Related Macular Degeneration | COMPLETED | PHASE1 | 2013-05 | 2014-11 | 2014-11 |
| NCT01858701 | Visual Performance Investigation of Two Toric Soft Contact Lenses | COMPLETED | NA | 2013-05 | 2013-10 | 2013-10 |
| NCT01833117 | Efficacy and Safety Study of FID 119515A | COMPLETED | NA | 2013-05 | 2013-06 | 2013-06 |
| NCT01809197 | Silicone Hydrogel Contact Lens Clinical and Comfort Benefits With a Multi-Purpose Disinfecting Solution | COMPLETED | NA | 2013-04 | 2013-07 | 2013-07 |
| NCT01839318 | Subjective Comparison of Pre-Lens Tear Film Stability With Daily Disposable Contact Lenses | COMPLETED | NA | 2013-04 | 2013-06 | 2013-06 |
| NCT02100410 | On-Eye Evaluation of Contact Lens Axis Location | COMPLETED | NA | 2013-04 | 2013-04 | 2013-04 |
| NCT01796964 | Efficacy and Safety Study of ESBA1008 Versus EYLEA® | COMPLETED | PHASE2 | 2013-03 | 2014-08 | 2013-10 |
| NCT01733732 | SYSTANE® BALANCE Symptoms (OSDI) & Inflammatory Biomarkers | COMPLETED | NA | 2013-03 | 2013-10 | 2013-10 |
| NCT01797783 | Clinical Evaluation of the Safety and Efficacy of a New Multifocal Contact Lens | COMPLETED | NA | 2013-02 | 2013-04 | 2013-04 |
| NCT01782482 | A Comparison of Two Color Contact Lenses in Habitual Clear Contact Lens Wearers | COMPLETED | NA | 2013-02 | 2013-04 | 2013-04 |
| NCT02055404 | On-Eye Evaluation of Contact Lens Rotation Marks | COMPLETED | NA | 2013-02 | 2013-02 | 2013-02 |
| NCT01733745 | SYSTANE® Family - Meibomian Deficiency | COMPLETED | NA | 2013-02 | 2013-06 | 2013-06 |
| NCT01696383 | Assessing the Efficacy of DuoTrav as a Replacement Therapy in Glaucoma Patients in Russia | WITHDRAWN | PHASE4 | 2013-02 | 2013-02 | 2013-02 |
| NCT01658839 | Pharmacokinetic and Safety Study of Travoprost 0.004% in Pediatric Glaucoma Patients | COMPLETED | PHASE1 | 2013-01 | 2013-07 | 2013-07 |
| NCT01743027 | Efficacy and Safety of an Ophthalmic Solution in Patients With Allergic Conjunctivitis | COMPLETED | PHASE3 | 2013-01 | 2013-07 | 2013-07 |
| NCT01699750 | Comparative In-Vivo Wetting Characteristics of Silicone Hydrogel Materials With Selected Lens Care Systems | COMPLETED | NA | 2012-12 | 2013-11 | 2013-11 |
| NCT01688726 | Evaluation of SYSTANE® BALANCE in Dry Eye Subjects With Lipid Deficiency | COMPLETED | NA | 2012-12 | 2013-11 | 2013-11 |
| NCT01684007 | A Clinical Outcome Study of Two Multifocal Intraocular Lenses (IOL) in Cataract Patients | COMPLETED | NA | 2012-11 | 2013-08 | 2013-08 |
| NCT01684033 | Evaluation of the Effectiveness of Two Marketed Multi-Purpose Solutions for Silicone Hydrogel Contact Lenses - Study 1 | COMPLETED | NA | 2012-11 | 2013-03 | 2013-03 |
| NCT01684046 | Evaluation of the Effectiveness of Two Marketed Multi-Purpose Solutions for Silicone Hydrogel Contact Lenses - Study 2 | COMPLETED | NA | 2012-11 | 2013-03 | 2013-03 |
| NCT01698814 | A Six-Week Safety Study of an Investigational Ophthalmic Solution | COMPLETED | PHASE3 | 2012-10 | 2013-01 | 2013-01 |
| NCT01997216 | Multifocal Lens Design Evaluation | COMPLETED | NA | 2012-10 | 2012-11 | 2012-11 |
| NCT01664039 | An Efficacy and Tolerability Study of TRAVATAN® Versus LUMIGAN® | COMPLETED | PHASE4 | 2012-09 | 2014-06 | 2014-06 |
| NCT01652664 | Study of Travoprost Ophthalmic Solution, 0.004% Compared to Timolol (0.5% or 0.25%) in Pediatric Glaucoma Patients | COMPLETED | PHASE3 | 2012-09 | 2014-03 | 2014-03 |
| NCT01629706 | Determination of Cell Population in Solution-Induced Corneal Staining (SICS) and Symptomatic Versus Asymptomatic Lens Wearers | COMPLETED | NA | 2012-09 | 2014-01 | 2014-01 |
| NCT01697969 | Confocal Analysis of Corneal Structures of Symptomatic Allergic Conjunctivitis Patients | COMPLETED | PHASE4 | 2012-09 | 2013-07 | 2013-07 |
| NCT01718028 | The Effect of SYSTANE® BALANCE on Tear Film Break Up Time in Dry Eye Subjects | COMPLETED | NA | 2012-09 | 2012-10 | 2012-10 |
| NCT01699087 | A Safety and Effectiveness Study of PRK Using the ALLEGRETTO WAVE® EYE-Q Excimer Laser System | COMPLETED | NA | 2012-08 | 2015-07 | 2015-07 |
| NCT01634659 | Clinical Evaluation of Two Daily Disposable Silicone Hydrogel Contact Lenses | COMPLETED | NA | 2012-07 | 2012-09 | 2012-09 |
| NCT01636986 | A Prospective Study of Two Daily Disposable Contact Lenses | COMPLETED | NA | 2012-07 | 2012-11 | 2012-11 |
| NCT01514721 | Efficacy of Changing to DuoTrav® (Travoprost 0.004%/Timolol 0.5% BAK-Free Fixed Combination) From Prior Therapy | TERMINATED | PHASE4 | 2012-06 | 2013-11 | 2013-11 |
| NCT01635933 | A Comparison of AIR OPTIX® COLORS Versus FRESHLOOK® COLORBLENDS | COMPLETED | NA | 2012-06 | 2012-09 | 2012-09 |
| NCT01614678 | A Comparison of Manufacturing Processes for AIR OPTIX® COLORS Contact Lens | COMPLETED | NA | 2012-06 | 2012-08 | 2012-08 |
| NCT01635920 | A Comparison of Silicone Hydrogel Contact Lenses: AIR OPTIX® COLORS Versus AIR OPTIX® AQUA | COMPLETED | NA | 2012-06 | 2012-08 | 2012-08 |
| NCT01603043 | A Multicenter, Proof-Of-Concept Study Of Intravitreal AL-78898A In Patients With Geographic Atrophy (GA) Associated With Age-Related Macular Degeneration (AMD) | TERMINATED | PHASE2 | 2012-06 | 2012-11 | 2012-11 |
| NCT01614600 | Clinical Evaluation of a Daily Disposable Contact Lens in Symptomatic Weekly/Monthly Lens Wearers | COMPLETED | NA | 2012-06 | 2012-09 | 2012-09 |
| NCT01605877 | AcrySof® IQ ReSTOR® +2.5 D Multifocal Intraocular Lens (IOL) Model SN6AD2 [SV25T0] in Japan | COMPLETED | NA | 2012-05 | 2013-12 | 2013-12 |
| NCT01573910 | An Evaluation of the Safety and Efficacy of Moxifloxacin Ophthalmic Solution 0.5% ((VIGAMOX®) Versus Ofloxacin Ophthalmic Solution 0.3% in the Treatment of Bacterial Conjunctivitis in Chinese Patients | COMPLETED | PHASE3 | 2012-05 | 2014-04 | 2014-04 |
| NCT01561560 | Clinical Evaluation of Two Daily Disposable Silicone Hydrogel Contact Lenses | COMPLETED | NA | 2012-05 | 2012-08 | 2012-08 |
| NCT01556893 | Creating LASIK Flaps With the LenSx Femtosecond Laser | COMPLETED | PHASE1 | 2012-04 | 2013-03 | 2013-03 |
| NCT01594294 | An Evaluation of Marketed Contact Lens Disinfectant Systems on Eyelid Tissues | COMPLETED | NA | 2012-04 | 2013-06 | 2013-06 |
| NCT01535560 | Safety and Efficacy Evaluation of Topical AL-60371 Otic Suspension, 0.3% in the Treatment of Acute Otitis Externa | COMPLETED | PHASE3 | 2012-04 | 2012-10 | 2012-10 |
| NCT01859702 | Pharmacokinetic Evaluation of Moxifloxacin in Vigadexa® in Aqueous Humor Samples Following Preoperative Antibiotic/Steroid Dosing in Cataract Surgery Patients | COMPLETED | PHASE4 | 2012-04 | 2012-08 | 2012-08 |
| NCT01535599 | Safety and Efficacy Evaluation of Topical AL-60371 Otic Suspension, 0.3% in the Treatment of Acute Otitis Externa | COMPLETED | PHASE3 | 2012-03 | 2013-05 | 2013-05 |
| NCT01514734 | Assessing the Efficacy and Tolerability of AZARGA® (Brinzolamide 1%/Timolol 0.5% Fixed Combination) as Replacement Therapy in Patients on COMBIGAN® (Brimonidine 0.2%/Timolol 0.5% Fixed Combination) Therapy in Brazil | TERMINATED | PHASE4 | 2012-03 | 2012-08 | 2012-08 |
| NCT01548833 | Pre-Lens Tear Film Performance of Silicone Hydrogel Daily Disposable Contact Lenses | COMPLETED | NA | 2012-03 | 2012-04 | 2012-04 |
| NCT01510717 | Clinical Investigation of AcrySof® IQ ReSTOR® +2.5 D Multifocal Intraocular Lens (IOL) Model SN6AD2 [SV25T0] | COMPLETED | NA | 2012-02 | 2012-12 | 2012-12 |
| NCT01510145 | Efficacy of Changing to TRAVATAN® From Prior Therapy | COMPLETED | PHASE4 | 2012-02 | 2013-05 | 2013-05 |
| NCT01479374 | Efficacy and Safety of AL-4943A Ophthalmic Solution in Patients With Allergic Conjunctivitis Using the Conjunctival Allergen Challenge (CAC) Model | COMPLETED | PHASE3 | 2012-01 | 2012-03 | 2012-03 |
| NCT01510132 | Travacom Post Marketing Surveillance Study | WITHDRAWN | PHASE4 | 2012-01 | 2012-01 | 2012-01 |
| NCT01493427 | Efficacy of Changing to TRAVATAN® From Prior Therapy | COMPLETED | PHASE4 | 2011-12 | 2013-02 | 2013-02 |
| NCT01518244 | Assessing the Efficacy and Tolerability of AZARGA® (Brinzolamide 1%/Timolol 0.5% Fixed Combination) as Replacement Therapy in Patients on Brimonidine 0.2%/Timolol 0.5% Fixed Combination Therapy (COMBIGAN®) in Latin America | COMPLETED | PHASE4 | 2011-12 | 2013-02 | 2013-02 |
| NCT01461811 | Prospective Study of an Investigational Toric Soft Contact Lens | COMPLETED | NA | 2011-12 | 2012-04 | 2012-04 |
| NCT01494545 | Performance Evaluation of DAILIES® TOTAL1™ in First Time Contact Lens Wearers | COMPLETED | NA | 2011-12 | 2012-04 | 2012-04 |
| NCT01497067 | Long Term Safety Protocol for the AcrySof CACHET Phakic Lens | COMPLETED | NA | 2011-11-21 | 2018-06-15 | 2018-06-15 |
| NCT01453855 | Travoprost 3-Month Safety and Efficacy Study | COMPLETED | PHASE3 | 2011-11 | 2012-08 | 2012-08 |
| NCT01494818 | Evaluation of Marketed Contact Lens Disinfectant Systems on Eyelid Tissues | COMPLETED | NA | 2011-11 | 2012-07 | 2012-07 |
| NCT01473160 | Daily Disposable Contact Lens Tear Film Study | COMPLETED | NA | 2011-11 | 2011-12 | 2011-12 |
| NCT01452009 | Three Month Safety and Efficacy Study of TRAVATAN® Versus Travoprost Ophthalmic Solution, 0.004% | WITHDRAWN | PHASE3 | 2011-11 | 2011-12 | 2011-12 |
| NCT01464424 | Assessment of Intraocular Pressure (IOP) Control in Subjects With Open-Angle Glaucoma or Ocular Hypertension Treated With Travoprost 0.004% (TRAVATAN® Z) or Bimatoprost 0.01% (LUMIGAN®) | COMPLETED | PHASE4 | 2011-10 | 2012-06 | 2012-06 |
| NCT01454505 | Safety and Efficacy of AL-53817 Nasal Spray Solution | COMPLETED | PHASE1 | 2011-10 | 2012-03 | 2012-03 |
| NCT01446835 | Asian Clinical Evaluation of an Investigational Contact Lens for Cosmetic Effect | COMPLETED | NA | 2011-10 | 2011-11 | 2011-11 |
| NCT01415401 | Efficacy and Tolerability of AZARGA® as Replacement Therapy in Patients on COMBIGAN® Therapy in Canada | COMPLETED | PHASE4 | 2011-09 | 2013-06 | 2013-06 |
| NCT01440322 | AIR OPTIX® COLORS Registration Trial | COMPLETED | NA | 2011-09 | 2012-01 | 2012-01 |
| NCT01340014 | Patient Preference Comparison of AZARGA Versus COSOPT | COMPLETED | PHASE4 | 2011-09 | 2012-10 | 2012-10 |
| NCT01445652 | A Lifestyle Investigation With Spectacles and Daily Disposable Contact Lenses in Young Patients | COMPLETED | NA | 2011-09 | 2012-06 | 2012-06 |
| NCT01426867 | A Comfort Study of Brinzolamide 1% / Brimonidine 0.2% Fixed Combination, Brinzolamide 1% and Brimonidine 0.2% | COMPLETED | PHASE2 | 2011-09 | 2011-11 | 2011-11 |
| NCT01327599 | Efficacy of Changing to DUOTRAV® From Prior Therapy | COMPLETED | PHASE4 | 2011-08 | 2012-11 | 2012-11 |
| NCT01433549 | Lens Wear Schedules and End-of-Day Comfort | COMPLETED | NA | 2011-08 | 2012-03 | 2012-03 |
| NCT01423773 | Ocular Comfort and OCT Observation of Post Lens Clearance and Ocular Tissue Compression | COMPLETED | NA | 2011-08 | 2011-12 | 2011-12 |
| NCT01424189 | Clinical Investigation of AcrySof® IQ ReSTOR® +3.0 D Multifocal Toric Intraocular Lens (IOL) | COMPLETED | NA | 2011-07 | 2013-01 | 2013-01 |
| NCT01398787 | Evaluation of the Cosmetic Performance of AIR OPTIX® COLORS | COMPLETED | NA | 2011-07 | 2011-12 | 2011-12 |
| NCT01426854 | Nepafenac Compared to Placebo for Ocular Pain and Inflammation | COMPLETED | PHASE3 | 2011-07 | 2012-04 | 2012-04 |
| NCT01382225 | Sodium Hyaluronate Ophthalmic Solution, 0.18% for Treatment of Dry Eye Syndrome | COMPLETED | PHASE3 | 2011-07 | 2012-05 | 2012-05 |
| NCT01417013 | Comparative Efficacy of SYSTANE® ULTRA vs Optive™ in Improving Tear Film Break-up Time | WITHDRAWN | NA | 2011-07 | 2012-01 | 2012-01 |
| NCT01318252 | AL-54478 Proof of Concept Study | COMPLETED | PHASE2 | 2011-06 | 2011-10 | 2011-10 |
| NCT01312454 | Safety and Intraocular Pressure (IOP) Lowering Effect of AL-59412C | TERMINATED | PHASE2 | 2011-06 | 2012-01 | 2012-01 |
| NCT01157065 | Evaluation of AL-78898A in Exudative Age-Related Macular Degeneration | COMPLETED | PHASE2 | 2011-06 | 2012-04 | 2012-04 |
| NCT01338610 | ESBA105 in Patients With Severe Dry Eye | COMPLETED | PHASE2 | 2011-06 | 2012-02 | 2012-02 |
| NCT01476722 | Lens Wearing Experience and Biocompatibility of a Multi-Purpose Disinfecting Solution (MPDS) | COMPLETED | NA | 2011-06 | 2011-10 | 2011-10 |
| NCT01371539 | Clinical Comparison of Two Multifocal Contact Lenses Made of Silicone Hydrogel Materials | COMPLETED | NA | 2011-06 | 2011-08 | 2011-08 |
| NCT01323777 | AcrySof® IQ ReSTOR® +3.0 D Multifocal Toric Intraocular Lens (IOL) Clinical Study in Japan | COMPLETED | NA | 2011-05 | 2013-03 | 2013-03 |
| NCT01309204 | Brinzolamide/Brimonidine Twice a Day (BID) Fixed Combination (FC) vs Brinzolamide BID Plus Brimonidine BID in Patients With Open Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2011-05 | 2013-01 | 2013-01 |
| NCT01310777 | Brinzolamide/Brimonidine Twice a Day (BID) Fixed Combination (FC) vs Brinzolamide BID and Brimonidine BID in Patients With Open Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2011-05 | 2013-01 | 2013-01 |
| NCT01484951 | AZARGA Transition Study in Taiwan for Patients With Uncontrolled Intraocular Pressure | COMPLETED | PHASE4 | 2011-05 | 2012-03 | 2012-03 |
| NCT01379768 | Study of the Cell Response in the Tear Film After Overnight Contact Lens Wear | COMPLETED | NA | 2011-05 | 2012-01 | 2012-01 |
| NCT01371552 | Performance Evaluation of a New Daily Disposable Silicone Hydrogel Lens | COMPLETED | NA | 2011-05 | 2011-08 | 2011-08 |
| NCT01272089 | A Study of Patient Perception and Quality of Life Associated With the Use of Olopatadine 0.2% in Subjects With Allergic Conjunctivitis | COMPLETED | PHASE4 | 2011-05 | 2011-12 | 2011-12 |
| NCT01362894 | Clinical Comparison of Two Daily Disposable Toric Lenses | COMPLETED | NA | 2011-05 | 2011-08 | 2011-08 |
| NCT01362907 | Clinical Comparison of Silicone Hydrogel and HEMA-based Daily Disposable Contact Lenses | COMPLETED | NA | 2011-05 | 2011-06 | 2011-06 |
| NCT01290068 | Visual Outcomes After Cataract Surgery: Multifocal AcrySof® IQ ReSTOR® Intraocular Lenses Versus Monofocal Intraocular Lenses | COMPLETED | NA | 2011-04 | 2012-10 | 2012-10 |
| NCT01326858 | Safety and Comfort of AL-4943A Ophthalmic Solution | COMPLETED | PHASE1 | 2011-04 | 2011-06 | 2011-06 |
| NCT01338402 | Evaluation of the Performance of AIR OPTIX® COLORS | COMPLETED | NA | 2011-04 | 2012-03 | 2012-03 |
| NCT01263444 | Safety and Efficacy of Adding AZARGA® Adjunctive to Prostaglandin Therapy | COMPLETED | PHASE4 | 2011-03 | 2013-04 | 2013-04 |
| NCT01225926 | A Comparison of Aspheric Toric Intraocular Lens (IOL) Implantation Versus Aspheric Non-Toric Lens Implantation | COMPLETED | NA | 2011-03 | 2012-06 | 2012-06 |
| NCT01297920 | Three Month Efficacy/Safety Study With a 3-Month Safety Extension of Brinzolamide 1%/Brimonidine 0.2% vs. Brinzolamide 1% or Brimonidine 0.2% | COMPLETED | PHASE3 | 2011-03 | 2012-06 | 2012-06 |
| NCT01318499 | Nepafenac 0.3% Two Study | COMPLETED | PHASE2 | 2011-03 | 2011-09 | 2011-09 |
| NCT01368198 | Evaluation of Extended Tear Film Break Up Time (TFBUT) With an Ocular Emulsion | COMPLETED | NA | 2011-03 | 2011-06 | 2011-06 |
| NCT01299155 | A Comparison of Visual Function After Bilateral Implantation of Presbyopia Correcting Intraocular Lenses | COMPLETED | NA | 2011-03 | | 2011-09 |
| NCT01298687 | Divided Dose of TRAVATAN® | COMPLETED | PHASE2 | 2011-02 | 2011-04 | 2011-04 |
| NCT01336569 | Safety and Efficacy of Changing to DuoTrav in Patients Uncontrolled on Timolol | COMPLETED | PHASE4 | 2011-02 | 2012-03 | 2012-03 |
| NCT01297517 | Efficacy and Safety Study of Brinzolamide 1%/Brimonidine 0.2% vs. Brinzolamide 1% and Brimonidine 0.2% | COMPLETED | PHASE3 | 2011-02 | 2012-03 | 2012-03 |
| NCT01276223 | Evaluation of Anti-Inflammatory Treatment in Dry Eye Patients | COMPLETED | PHASE2 | 2011-02 | 2012-01 | 2012-01 |
| NCT01484938 | Lens Wearing Experience and Biocompatibility of a Marketed Multi-Purpose Disinfecting Solution in Silicone Hydrogel and Soft Contact Lens Wearers | COMPLETED | NA | 2011-02 | 2011-05 | 2011-05 |
| NCT01300767 | Four Week Performance Comparison Between Two Commercially Available Silicone Hydrogel Lenses | COMPLETED | NA | 2011-02 | 2011-04 | 2011-04 |
| NCT01300741 | One Month Performance Comparison Between Two Commercially Available Silicone Hydrogel Lenses | COMPLETED | NA | 2011-02 | 2011-04 | 2011-04 |
| NCT01483989 | In Vivo Measurement of Corneal Epithelial Changes in Dry Eye Patients | COMPLETED | NA | 2011-02 | 2011-06 | 2011-06 |
| NCT01295905 | Prospective Study of an Investigational Daily Disposable Contact Lens | COMPLETED | NA | 2011-01 | 2011-05 | 2011-05 |
| NCT01294956 | A Clinical Evaluation of an Investigational Lubricant Eye Gel (FID 115958D) | COMPLETED | NA | 2011-01 | 2011-04 | 2011-04 |
| NCT01238783 | Safety and Efficacy of AL-15469A 0.5% / AL-6515 0.3% Ophthalmic Suspension for Treatment of Bacterial Conjunctivitis | WITHDRAWN | PHASE2 | 2011-01 | | 2011-12 |
| NCT01282138 | Assessment of Alcon's Ocular Image Quantification System | COMPLETED | PHASE4 | 2010-12 | 2011-03 | 2011-03 |
| NCT01482312 | Effect of Contact Lenses on Tear Osmolarity in a Controlled Low Humidity Chamber | COMPLETED | NA | 2010-12 | 2011-02 | 2011-02 |
| NCT01293240 | Prospective Study of Lens Performance of a Monthly Replacement Lens at Two Weeks and Four Weeks | COMPLETED | NA | 2010-12 | 2011-04 | 2011-04 |
| NCT01342107 | Effect of FID 114675A on Lens Wettability | COMPLETED | NA | 2010-12 | 2011-02 | 2011-02 |
| NCT01268501 | Clinical Assessment of a Multifocal Contact Lens for People Who Use Reading Glasses Only | COMPLETED | NA | 2010-12 | 2011-02 | 2011-02 |
| NCT01254760 | Comparison of Two Multifocal Contact Lenses Worn on a Daily Disposable Basis | COMPLETED | NA | 2010-12 | 2011-01 | 2011-01 |
| NCT01257217 | A Comparison of Visual Function After Bilateral Implantation of Presbyopia-Correcting Intraocular Lenses (IOLs) | COMPLETED | NA | 2010-11 | 2011-06 | 2011-06 |
| NCT01357616 | Fixed Combination Brinzolamide 1%/Timolol 0.5% Versus Brinzolamide 1% + Timolol 0.5% in Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2010-11 | 2013-01 | 2013-01 |
| NCT01252134 | Evaluation of Silicone Hydrogel Lens Wettability With Marketed Lens Care Solutions | COMPLETED | NA | 2010-11 | 2011-02 | 2011-02 |
| NCT01254747 | Clinical Evaluation of an Investigational Soft Contact Lens | COMPLETED | NA | 2010-11 | 2010-12 | 2010-12 |
| NCT01311609 | A Multi-Site Post Marketing Surveillance Study for Systane in Indian Patients | COMPLETED | PHASE4 | 2010-11 | 2011-07 | 2011-07 |
| NCT01304693 | ESBA1008 Safety, Tolerability and Effects in Wet Age-Related Macular Degeneration (AMD) Patients | COMPLETED | PHASE1, PHASE2 | 2010-10 | 2013-03 | 2013-03 |
| NCT01201798 | Safety and Efficacy of Difluprednate 0.05% for the Treatment of Anterior Uveitis | COMPLETED | PHASE3 | 2010-10 | 2011-08 | 2011-08 |
| NCT01240135 | Clinical Performance of a Silicone Hydrogel Lens With Use of FID 114675A | COMPLETED | NA | 2010-10 | 2011-02 | 2011-02 |
| NCT01252121 | Residence Time Evaluation of Systane Ultra Lubricant Eye Drops vs. Hialid and Saline | COMPLETED | NA | 2010-10 | 2011-06 | 2011-06 |
| NCT01230736 | Safety and Efficacy of Changing to DuoTrav From Prior Therapy | COMPLETED | PHASE4 | 2010-10 | 2011-02 | 2011-02 |
| NCT01233076 | Clinical Comparison of Two Daily Disposable Contact Lenses in a Population of Daily Disposable Contact Lens Wearers | COMPLETED | NA | 2010-10 | 2010-11 | 2010-11 |
| NCT01250054 | Comparison of Two Multifocal Contact Lenses | COMPLETED | NA | 2010-10 | 2010-10 | 2010-10 |
| NCT01211535 | Subjective Comfort With Multipurpose Care Solutions in Soft Contact Lens Wearers | COMPLETED | NA | 2010-09 | 2010-11 | 2010-11 |
| NCT01199510 | Efficacy Evaluation of SYSTANE® ULTRA in Patients Scheduled for Cataract Surgery | COMPLETED | PHASE4 | 2010-09 | 2011-06 | 2011-06 |
| NCT01207466 | Evaluation of Two Daily Disposable Contact Lenses for Wearers With Astigmatism | COMPLETED | NA | 2010-09 | 2010-10 | 2010-10 |
| NCT01198782 | Evaluating Safety and Efficacy of FID 112903 Post Discontinuation of Long-term Use of RESTASIS® (Cyclosporine Ophthalmic Emulsion) 0.05% | COMPLETED | PHASE4 | 2010-09 | 2011-05 | 2011-05 |
| NCT01471158 | Patient Preference Comparison of AZARGA Versus COSOPT in Patients With Glaucoma | COMPLETED | PHASE4 | 2010-09 | 2011-05 | 2011-05 |
| NCT01294969 | Patient Perception Study for AL-4943A | COMPLETED | PHASE4 | 2010-09 | 2011-10 | 2011-10 |
| NCT01233089 | Fitting Children With Contact Lenses | COMPLETED | NA | 2010-09 | 2011-08 | 2011-08 |
| NCT01200511 | Pilot Study of AcrySof® IQ ReSTOR® +3.0 D Multifocal Toric Intraocular Lens (IOL) | COMPLETED | NA | 2010-08 | 2011-09 | 2011-09 |
| NCT01124045 | Difluprednate Pediatric Study for the Treatment of Inflammation Post-Cataract Surgery | COMPLETED | PHASE3 | 2010-08 | 2012-04 | 2012-04 |
| NCT01223040 | An Open-Label, Single-Center Study Evaluating the Effect of Systane Balance on Video Ocular Protection Index (OPI) and Blink Patterns in Patients Diagnosed With Dry Eye | COMPLETED | NA | 2010-08 | | 2010-09 |
| NCT01190631 | An Assessment of Residual Spherical Aberration, Postoperative Total High Order Aberrations, and Functional Vision Correlation Following Intraocular Lens (IOL) Implantation | COMPLETED | NA | 2010-07 | | 2011-11 |
| NCT01198600 | Ocular Comfort and the "Aging" Lens (ERBIUM) | COMPLETED | NA | 2010-07 | 2011-07 | 2011-07 |
| NCT01187355 | Alcon Multi-Purpose Disinfecting Solution Versus Renu Fresh Multi-Purpose Solution in Symptomatic Contact Lens Wearers | COMPLETED | NA | 2010-07 | 2011-01 | 2011-01 |
| NCT01159756 | To Assess the Safety and Efficacy of Travacom in Patients With Uncontrolled Intraocular Pressure | COMPLETED | PHASE4 | 2010-07 | 2011-11 | 2011-11 |
| NCT01160133 | To Evaluate the Physical Effects of Systane(R) Lubricant Eye Drops Compared to Refresh Tears(R) Lubricant Eye Drops | COMPLETED | NA | 2010-07 | 2011-06 | 2011-06 |
| NCT01086774 | Efficacy of Systane Balance to Stabilize the Tear Film in Dry Eye Subjects | COMPLETED | PHASE4 | 2010-07 | | 2010-11 |
| NCT01185834 | Assessment of Lotrafilcon A Contact Lenses | COMPLETED | NA | 2010-07 | 2010-12 | 2010-12 |
| NCT01166971 | A Comparison of Visual Function After Bilateral Implantation of Presbyopia-correcting Intraocular Lenses (IOLs) | COMPLETED | PHASE4 | 2010-07 | | 2011-03 |
| NCT00992563 | WALTZ - Wet Age-Related Macular Degeneration (AMD) AL-39324 Treatment Examination | COMPLETED | PHASE2 | 2010-06 | 2011-05 | 2011-05 |
| NCT01109173 | Confirmatory Study Nepafenac 0.3% | COMPLETED | PHASE3 | 2010-06 | | 2011-05 |
| NCT01192321 | Visual Outcomes After Bilateral Surgical Cataract Phacoemulsification: AcrySof Toric IOL Implantation Compared to Monofocal IOL Implantation | TERMINATED | PHASE4 | 2010-06 | 2010-12 | 2010-12 |
| NCT01164865 | Subjective Comfort With Multipurpose and Hydrogen Peroxide Lens Care Solutions in Soft Contact Lens Wearers | COMPLETED | NA | 2010-06 | 2010-12 | 2010-12 |
| NCT01159769 | Patient Perceptions and Quality of Life Associated With the Use of Olapatadine 0.2% for the Treatment of Allergic Conjunctivitis | COMPLETED | PHASE4 | 2010-06 | 2010-08 | 2010-08 |
| NCT01165164 | An Evaluation of the Nighttime Retention of Effect of an Investigational Lubricant Eye Drop (FID 115958D) | COMPLETED | NA | 2010-06 | 2010-07 | 2010-07 |
| NCT01155726 | The Effect of Masking on Subjective Results During Daily Disposable Contact Lens Studies | COMPLETED | NA | 2010-05 | 2011-02 | 2011-02 |
| NCT01139372 | An Evaluation of the Daytime Use of an Investigational Lubricant Eye Drop | COMPLETED | NA | 2010-05 | 2010-06 | 2010-06 |
| NCT01134211 | Clinical Comparison of Two Daily Disposable Lenses Among Daily Disposable Lens Wearers | COMPLETED | NA | 2010-05 | 2010-07 | 2010-07 |
| NCT01105585 | A Comparative Pilot Study Of High-Order Aberrations With Aspheric IOL Models SN60WF and ZCB00 | COMPLETED | NA | 2010-04 | | 2011-06 |
| NCT01132287 | An Evaluation of a Marketed Lubricated Eye Drop in Soft Contact Lens Wearers Who Experience Ocular Dryness | COMPLETED | NA | 2010-04 | 2010-11 | 2010-11 |
| NCT01111890 | Comparison of the Efficacy of AZARGA® Versus COSOPT® in Patients With Open-Angled Glaucoma or Ocular Hypertension | COMPLETED | PHASE4 | 2010-04 | 2011-07 | 2011-07 |
| NCT01114893 | Travoprost Five Day Posology Study | COMPLETED | PHASE2 | 2010-04 | | 2010-05 |
| NCT01102244 | A Study to Evaluate the Clinical Efficacy and Safety of Tobradex® ST Compared to Azasite® in the Treatment of Subjects With Moderate to Severe Chronic Blepharitis | COMPLETED | PHASE3 | 2010-04 | | 2010-06 |
| NCT01119287 | Assessing the Efficacy of Maxidex® and Patanol® for the Treatment of Allergic Conjunctivitis | COMPLETED | PHASE4 | 2010-03 | 2010-09 | 2010-09 |
| NCT01100424 | Assessment of Tear Film-Based Proteins Associated With Care Solution Induced Corneal Staining | COMPLETED | NA | 2010-03 | 2010-09 | 2010-09 |
| NCT01055366 | ELAZOP Switching Study in Korea | COMPLETED | PHASE4 | 2010-03 | 2011-12 | 2011-12 |
| NCT00912054 | DuoTrav APS Versus XALACOM® in Ocular Surface Health | TERMINATED | PHASE3 | 2010-03 | 2011-05 | 2011-05 |
| NCT01097863 | Clinical Validation of the New Print on Focus DAILIES Toric | COMPLETED | NA | 2010-03 | 2010-05 | 2010-05 |
| NCT01100411 | Changes in Invitro and ex Vivo Lens Metrology With Daily Wear Contact Lenses | COMPLETED | NA | 2010-03 | 2010-07 | 2010-07 |
| NCT01109485 | Clinical Evaluation of 0.1% Olopatadine Hydrochloride Ophthalmic Solution in Pediatric Patients | COMPLETED | PHASE4 | 2010-03 | 2011-07 | 2011-07 |
| NCT01166659 | Study of CyPass Implantation In Patients With Open Angle Glaucoma Refractory to Single or Multi-agent Topical Therapy | COMPLETED | NA | 2010-02 | 2014-05 | 2013-05 |
| NCT01037179 | An Open-Label, Long-Term Study With AL-4943A Ophthalmic Solution, 0.2% in Patients With Allergic Conjunctivitis | COMPLETED | PHASE3 | 2010-02 | 2010-05 | 2010-05 |
| NCT01071902 | Safety and Efficacy of Moxidex Otic | TERMINATED | PHASE3 | 2010-02 | 2011-10 | 2011-10 |
| NCT01105910 | Efficacy of Systane Ultra in Post Menopausal Women With Dry Eye | COMPLETED | PHASE4 | 2010-02 | | 2010-12 |
| NCT01057966 | Bioavailability of Nutrients Contained in Softgel Capsules vs Tablets | COMPLETED | PHASE4 | 2010-02 | 2011-09 | 2011-09 |
| NCT01079858 | Evaluation of FID 114657 in Dry Eye Subjects | COMPLETED | NA | 2010-02 | | 2010-04 |
| NCT01079871 | Evaluation of FID 114657 in Sjogren's Syndrome Subjects | COMPLETED | NA | 2010-02 | | 2010-06 |
| NCT00872651 | Travoprost 0.004%/Timolol 0.5% Versus Latanoprost 0.005%/Timolol in Chinese Patients With Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2010-01 | 2011-11 | 2011-11 |
| NCT01066988 | Evaluation of an Investigational Lubricant Eye Drop on Lipid Layer Thickness | COMPLETED | NA | 2010-01 | | 2010-02 |
| NCT01077011 | Acute Comfort and Blur Profile of a Lubricant Eye Drop Versus a Marketed Lubricant Eye Gel | COMPLETED | NA | 2010-01 | | 2010-01 |
| NCT01070381 | Daily Disposable Toric Comparative Trial in Europe | COMPLETED | NA | 2010-01 | 2010-03 | 2010-03 |
| NCT01076998 | Acute Comfort and Blur Profile of a Lubricant Eye Drop Versus a Marketed Eye Ointment | COMPLETED | NA | 2010-01 | | 2010-01 |
| NCT01074606 | Visual Function After Implantation of AcrySof® Toric Lens | TERMINATED | PHASE4 | 2010-01 | | 2011-03 |
| NCT01001091 | AL-38583 Ophthalmic Solution for Allergic Conjunctivitis Associated Inflammation | COMPLETED | PHASE2 | 2009-12 | 2010-04 | 2010-04 |
| NCT01045733 | A Comparison of Corneal Aberrations in Subjects With Contralateral AcrySof IQ Toric Intraocular Lens (IOL) and AcrySof IQ IOL With Limbal Relaxing Incision (LRI) | COMPLETED | NA | 2009-12 | 2011-05 | 2011-05 |
| NCT01341990 | Effect of an Investigational Multi-Purpose Solution on Lens Moisture | COMPLETED | NA | 2009-11 | 2010-01 | 2010-01 |
| NCT01030237 | An Evaluation of the Safety and Efficacy of FID 114657 | COMPLETED | NA | 2009-11 | | 2010-01 |
| NCT01051804 | Evaluation of the Repeated Usage of Systane Ultra Eyedrop | COMPLETED | PHASE4 | 2009-11 | | 2010-07 |
| NCT01341977 | Safety and Efficacy of an Investigational Multi-Purpose Disinfecting Solution | COMPLETED | NA | 2009-11 | 2010-05 | 2010-05 |
| NCT00987272 | Study of Olopatadine HCl Ophthalmic Solutions Compared to Vehicle Using the Conjunctival Allergen Challenge (CAC) Model of Acute Allergic Conjunctivitis in Japanese Subjects | COMPLETED | PHASE3 | 2009-10 | 2009-11 | 2009-11 |
| NCT00961649 | Safety and Efficacy of Brinzolamide/Brimonidine Fixed Combination | TERMINATED | PHASE2 | 2009-10 | 2010-02 | 2010-02 |
| NCT01023464 | Tear Film Break-Up Time Evaluation of FID 114657 | COMPLETED | NA | 2009-10 | | 2010-01 |
| NCT01010555 | In-vivo Wettability Grading and Assessment Study | COMPLETED | NA | 2009-10 | 2010-04 | 2010-04 |
| NCT01007916 | Subjective Evaluation of a Commercially Marketed Contact Lens Amongst a Subset of the Contact Lens Wearing Population | COMPLETED | NA | 2009-10 | 2010-01 | 2010-01 |
| NCT01007812 | Clinical Comparison of Two Silicone Hydrogel Toric Lenses in the US | COMPLETED | NA | 2009-10 | 2009-11 | 2009-11 |
| NCT00710905 | Visual Function With Contralateral AcrySof® ReSTOR® Aspheric SN6AD1 and SN6AD3 | TERMINATED | PHASE4 | 2009-10 | 2010-09 | 2010-09 |
| NCT00724269 | Comparison of OPTI-FREE RepleniSH and ReNu Multi-Plus Lens Care Regimens on Corneal Epithelium | COMPLETED | NA | 2009-10 | 2011-07 | 2011-07 |
| NCT01016132 | Clinical Evaluation of a Silicone Hydrogel Lens | COMPLETED | NA | 2009-10 | 2009-12 | 2009-12 |
| NCT01085357 | Study of an Implantable Device for Lowering Intraocular Pressure in Glaucoma Patients Undergoing Cataract Surgery | COMPLETED | NA | 2009-09 | 2015-03 | 2015-03 |
| NCT00966940 | Efficacy and Safety of Travoprost 0.004% Versus Tafluprost 0.0015% in Patients With Primary Open-angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE4 | 2009-09 | 2010-03 | 2010-03 |
| NCT01035905 | Comparative Clinical Evaluation of Daily Disposable Lenses in Symptomatic Daily Disposable Lens Wearers | COMPLETED | NA | 2009-09 | 2009-12 | 2009-11 |
| NCT00979615 | Safety and Efficacy of Olopatadine 0.6% and Azelastine 137 Mcg in Vasomotor Rhinitis | COMPLETED | PHASE4 | 2009-09 | | 2009-11 |
| NCT00939276 | Macular Edema Incidence/Severity Reduction With Nevanac | TERMINATED | PHASE3 | 2009-08 | 2011-08 | 2011-05 |
| NCT00995189 | Clinical Evaluation of the Causes of Contact Lens Related Dry Eye | COMPLETED | NA | 2009-08 | 2010-04 | 2010-04 |
| NCT00987623 | Clinical Evaluation of Two Daily Disposable Lenses in Neophytes | COMPLETED | NA | 2009-08 | 2009-12 | 2009-12 |
| NCT00965237 | Multifocal Contact Lens Use in Previous Contact Lens Wearers With Near Vision Demands | COMPLETED | NA | 2009-08 | 2009-12 | 2009-12 |
| NCT00963560 | Presbyopia-Correcting Intraocular Lenses (IOLs) | COMPLETED | PHASE4 | 2009-08 | | 2011-03 |
| NCT00967473 | ACRYSOF® Toric NATURAL T9 Intraocular Lens (IOL) | COMPLETED | NA | 2009-08 | 2010-05 | 2010-05 |
| NCT00934102 | Ophthalmic Compatibility During Seven Days of Continuous Wear of Silicone Hydrogel Lenses | COMPLETED | NA | 2009-08 | 2009-09 | 2009-09 |
| NCT00928590 | Safety Study of DuoTrav APS in Patients With Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2009-07 | 2010-11 | 2010-11 |
| NCT00761709 | Safety and Intraocular Pressure (IOP)-Lowering Efficacy of AL-39256 in Patients With Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE2 | 2009-07 | 2009-10 | 2009-10 |
| NCT00966576 | Efficacy and Safety of Adding Azarga to Prostaglandin Monotherapy | COMPLETED | PHASE4 | 2009-07 | 2010-08 | 2010-08 |
| NCT00946777 | Barrier Function Measurement in Dry Eye Patients After Using Systane Ultra for 30 Days | COMPLETED | NA | 2009-07 | 2009-09 | 2009-09 |
| NCT00958828 | Clinical Evaluation of Two Daily Disposable Lenses in a Population of Daily Disposable (DD) Lens Wearers | COMPLETED | NA | 2009-07 | 2009-09 | 2009-09 |
| NCT00953407 | Comparative Clinical Evaluation of Daily Disposable Lenses in Symptomatic Lens Wearers | COMPLETED | NA | 2009-07 | 2009-09 | 2009-09 |
| NCT00983203 | Acute Comfort and Haze Profile of FID 114657 | COMPLETED | NA | 2009-07 | | 2009-08 |
| NCT00892762 | Travoprost APS Versus Xalatan® in Patient Reported Outcomes and Ocular Surface Health | COMPLETED | PHASE3 | 2009-06 | 2011-05 | 2011-05 |
| NCT00893139 | A Study of AL-38583 Ophthalmic Solution 0.05%, 0.010% Versus AL-38583 Vehicle for Dry Eye | COMPLETED | PHASE2 | 2009-06 | 2010-01 | 2010-01 |
| NCT00901693 | An Evaluation of the Efficacy and Safety of AL-46383A Ophthalmic Solution for the Treatment of Adenoviral Conjunctivitis | TERMINATED | PHASE2 | 2009-06 | 2010-07 | 2010-07 |
| NCT00940459 | Subjective and Conjunctival Response to Edge Design of Different Silicone Hydrogels | COMPLETED | NA | 2009-06 | 2009-09 | 2009-09 |
| NCT00938951 | Evaluate the Ability of Systane Ultra to Improve Subjective Symptoms of Ocular Irritation Post 60 Min. Athletic Performance. | COMPLETED | NA | 2009-06 | | 2009-07 |
| NCT00933166 | Assessing the Performance of Lotrafilcon A Lenses During a Three Month Period | COMPLETED | NA | 2009-06 | 2009-11 | 2009-11 |
| NCT00929747 | Comparison of Corneal Aberrations and Visual Outcomes in AcrySof IQ Toric Patients Versus Limbal Relaxing Incision (LRI) Patients | WITHDRAWN | PHASE4 | 2009-06 | 2009-10 | 2009-10 |
| NCT00929487 | Acute Clinical Evaluation of Multi-purpose Solutions (MPS) in Soft Contact Lens Wearers | COMPLETED | NA | 2009-05 | 2012-05 | 2012-05 |
| NCT00881673 | To Evaluate the Efficacy of AL-38583 in the Reduction of Tear Eosinophil Count Following Conjunctival Allergen Challenge | WITHDRAWN | PHASE2 | 2009-05 | 2009-05 | 2009-05 |
| NCT00909792 | Clinical Evaluation of Two New Silicone Hydrogel Multifocal Products | COMPLETED | NA | 2009-05 | 2009-06 | 2009-06 |
| NCT00931307 | Evaluation of Lotrafilcon A Lenses Over a Three Month Period | COMPLETED | NA | 2009-05 | 2009-09 | 2009-09 |
| NCT00890097 | Geographic Atrophy Treatment Evaluation | TERMINATED | PHASE3 | 2009-04 | 2012-05 | 2012-05 |
| NCT00982046 | A Clinical Comparison of Three Contact Lens Care Systems and Their Effect on Contact Lenses | COMPLETED | NA | 2009-04 | 2010-05 | 2010-05 |
| NCT00886119 | Comparison of a Multifocal Contact Lens to a Traditional Multifocal Contact Lens | COMPLETED | NA | 2009-04 | 2009-05 | 2009-05 |
| NCT00878839 | Investigation of Corneal Aberrations and Visual Outcomes in Patients Implanted With an AcrySof Toric Intraocular Lens (IOL) | WITHDRAWN | NA | 2009-03 | 2009-03 | 2009-03 |
| NCT00848536 | Efficacy Study of Travoprost APS Versus TRAVATAN | COMPLETED | PHASE3 | 2009-03 | 2010-01 | 2010-01 |
| NCT00884806 | 7-Day, Multi-Site Study of an Investigational Multi-Purpose Disinfecting Solution for Contact Lens Wearers | COMPLETED | NA | 2009-03 | 2009-06 | 2009-06 |
| NCT00885092 | Single Site Study of the Wettability of Contact Lenses With an Investigational Multi-Purpose Disinfecting Solution vs. a Marketed Multi-Purpose Solution | COMPLETED | NA | 2009-03 | 2009-05 | 2009-05 |
| NCT00862472 | Safety and Efficacy Study of DuoTrav APS Versus DuoTrav | WITHDRAWN | PHASE3 | 2009-03 | 2009-06 | 2009-06 |
| NCT00845195 | Comparison of Seasonal Allergic Rhinitis Treatment With 2 Antihistamines Used in Combination With Intranasal Corticosteroid | COMPLETED | PHASE4 | 2009-03 | | 2009-05 |
| NCT00840268 | A Study of Hydroxypropyl Guar Galactomannan 0.25% (HPGG) Versus Vehicle in Dry Eye Patients | COMPLETED | PHASE2 | 2009-02 | 2009-07 | 2009-07 |
| NCT00800540 | Circadian Ocular Perfusion Pressure and Ocular Blood Flow | COMPLETED | PHASE4 | 2009-02 | 2012-01 | 2012-01 |
| NCT00828906 | DuoTrav® Eye Drops As Replacement Therapy Program | COMPLETED | PHASE4 | 2009-02 | | 2009-11 |
| NCT00761995 | Safety and Efficacy of Brinzolamide Dosed TID With Dorzolamide Dosed TID in Reducing Intraocular Pressure in Patients With Open Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE4 | 2009-02 | 2010-07 | 2010-07 |
| NCT00840580 | Effect on Wound Healing of Vigamox Versus Cravit | COMPLETED | PHASE4 | 2009-01 | | 2009-09 |
| NCT00818844 | Role of Nepafenac in Reducing Macular Volume After Epiretinal Membrane Surgery | COMPLETED | PHASE4 | 2009-01 | 2010-06 | 2010-06 |
| NCT00848068 | Evaluation of FID 114657 on Tear Film Lipid Layer Thickness | COMPLETED | NA | 2009-01 | | 2009-03 |
| NCT00818909 | Systane Clinical Experience Study | COMPLETED | PHASE4 | 2009-01 | 2009-10 | 2009-10 |
| NCT00788541 | A Dose-Volume Study of a Treatment for Elevated IOP Due to Open-Angle Glaucoma or Ocular Hypertension | TERMINATED | PHASE2 | 2008-12 | 2009-09 | 2009-09 |
| NCT00798759 | Examination of Ocular Surface Effects With Administration of Travatan Z and XALATAN | COMPLETED | PHASE4 | 2008-12 | 2009-05 | 2009-05 |
| NCT00809198 | Kynex Versus Refresh Plus Study in Subject With Dry Eye | COMPLETED | PHASE4 | 2008-12 | 2009-05 | 2009-05 |
| NCT00823615 | Comparison of Two New Silicone Hydrogel Multifocal Products | COMPLETED | NA | 2008-12 | 2009-02 | 2009-02 |
| NCT00818116 | Visual Function Evaluation of Bilateral AcrySof ReSTOR Aspheric IOL | COMPLETED | PHASE4 | 2008-12 | | 2009-07 |
| NCT00813982 | Daily Wear Comparison of Enhanced and Non-Enhanced Silicone Hydrogel Lenses | COMPLETED | NA | 2008-11 | 2008-12 | 2008-12 |
| NCT00789555 | Safety of PATANASE Nasal Spray in Patients With Perennial Allergic Rhinitis | COMPLETED | PHASE4 | 2008-11 | 2011-01 | 2011-01 |
| NCT00799422 | Evaluation of Contact Lenses and Conjunctival Staining in Normal Patients | COMPLETED | NA | 2008-11 | 2009-03 | 2009-03 |
| NCT00782717 | A Clinical Safety and Efficacy Comparison of NEVANAC 0.1% to Vehicle After Cataract Surgery in Diabetic Retinopathy Patients | COMPLETED | PHASE2 | 2008-11 | 2010-07 | 2010-07 |
| NCT00810511 | Evaluation of Two Silicone Hydrogel Lenses Over a One Month Period | COMPLETED | NA | 2008-11 | 2009-01 | 2009-01 |
| NCT00808834 | Non-dispense Comfort Comparison of Two Silicone Hydrogel Lenses | COMPLETED | NA | 2008-11 | 2008-12 | 2008-12 |
| NCT00804791 | Residence Time Evaluation of Marketed OTC Ophthalmic Products | COMPLETED | NA | 2008-11 | | 2009-02 |
| NCT00759148 | Moxifloxacin AF Ophthalmic Solution for Treatment of Bacterial Conjunctivitis | COMPLETED | PHASE3 | 2008-10 | 2010-03 | 2010-03 |
| NCT00743249 | Punctal Plug Study to Determine the Safety and Retention Times of Various Lengths of Canalicular Stents in Volunteers | COMPLETED | NA | 2008-10 | 2009-02 | 2009-02 |
| NCT00761319 | Phase III Clinical Trial of TRAVATAN Z in Ocular Surface Health | COMPLETED | PHASE3 | 2008-10 | 2009-09 | 2009-09 |
| NCT00710931 | Visual Function With Bilateral AcrySof® ReSTOR® Aspheric SN6AD1 | COMPLETED | PHASE4 | 2008-10 | 2010-09 | 2010-09 |
| NCT00767481 | 1 Year Study Trav/Brinz QD Fixed Combination Versus COSOPT | TERMINATED | PHASE3 | 2008-10 | 2009-02 | 2009-02 |
| NCT00798577 | Study of the Progression of Bacterial Conjunctivitis Symptoms Upon Antibiotic Treatment | COMPLETED | PHASE4 | 2008-10 | 2009-02 | 2009-02 |
| NCT00772304 | Evaluation of the Sensory Attributes of Olopatadine 0.6% and Azelastine 137mcg Nasal Sprays in Patients w/Allergic Rhinitis | COMPLETED | PHASE4 | 2008-10 | | 2008-11 |
| NCT00794144 | Safety and Pharmacokinetics of Patanase in Pediatric Patients 2 to < 6 Years of Age | COMPLETED | PHASE2 | 2008-10 | | 2008-12 |
| NCT00767494 | Travoprost/Brinzolamide Fixed Combination Versus Travatan and Versus AZOPT | TERMINATED | PHASE3 | 2008-10 | 2009-02 | 2009-02 |
| NCT00772707 | A Multi-Center Investigation of Patient Acceptability of OPTI-FREE RepleniSH® Multi-Purpose Disinfecting Solution (MPDS) | COMPLETED | NA | 2008-09 | 2008-10 | 2008-10 |
| NCT00759239 | Phase IV Randomised Double-masked Clinical Trial: Assessing Morning Versus Evening Dosing of a Fixed Dose Combination of Travoprost 0.004% / Timolol Maleate 0.5% in Patients With Primary Open-angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE4 | 2008-09 | 2011-01 | 2011-01 |
| NCT00756093 | Acute Comfort and Blurring Profile Evaluation of Marketed Lubricant Eye Drops | COMPLETED | NA | 2008-09 | 2008-09 | 2008-09 |
| NCT00762606 | Phaco Versus Small Incision Cataract Surgery (SICS) Health Economic Study | COMPLETED | NA | 2008-09 | 2010-06 | 2010-06 |
| NCT00870103 | Study of Efficacy and Safety of Vigadexa in Treating Inflammation and Infection Post-cataract Surgery | COMPLETED | PHASE4 | 2008-09 | | 2009-02 |
| NCT00760045 | Clinical Pharmacological Study of AL-43546 Ophthalmic Product in Subjects With Shortened Tear Film Break Up Time | COMPLETED | PHASE2 | 2008-08 | | 2008-10 |
| NCT00690794 | Travatan Z in Ocular Surface Health in Patients With Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2008-07 | 2009-05 | 2009-05 |
| NCT00708422 | Effects of Travatan Z and Xalatan on Ocular Surface Health | COMPLETED | PHASE4 | 2008-07 | 2009-08 | 2009-08 |
| NCT00748865 | Acute Comfort and Blur of Systane Ultra and Systane | COMPLETED | NA | 2008-07 | 2008-08 | 2008-08 |
| NCT00818805 | Efficacy Investigation Study of Olopatadine Hydrochloride Ophthalmic Solution Using OHIO Chamber in Patients With Seasonal Allergic Rhinitis (SAR) | COMPLETED | PHASE4 | 2008-07 | | 2008-07 |
| NCT00760539 | Safety and Efficacy of Travoprost/Timolol BAC-free | COMPLETED | PHASE3 | 2008-06 | 2008-12 | 2008-12 |
| NCT00691717 | Anecortave Acetate Safety in Patients With Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE2, PHASE3 | 2008-06 | 2009-09 | 2009-09 |
| NCT00750633 | A Phase III Study of an Otic Formulation in Acute Otitis Externa | COMPLETED | PHASE3 | 2008-06 | 2009-01 | 2009-01 |
| NCT00702377 | Evaluation of SYSTANE Ultra Lubricant Eye Drops | COMPLETED | NA | 2008-06 | 2008-09 | 2008-09 |
| NCT00760058 | Visual Outcome and Visual Quality After Bilateral Implantation of the AcrySof® IQ IOL Compared to MI60® and Tecnis® IOL | WITHDRAWN | PHASE4 | 2008-06 | 2010-12 | 2010-12 |
| NCT00695435 | Tobramycin Tear Concentrations | COMPLETED | PHASE1 | 2008-06 | | 2008-06 |
| NCT00672997 | A Phase III Study of Travoprost/Timolol Combination in Patients With Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2008-05 | 2008-12 | 2008-12 |
| NCT00673764 | The Effect of Systane Ultra Lubricant Eye Drops (FID 112903) on Visual Performance | COMPLETED | NA | 2008-05 | 2008-06 | 2008-06 |
| NCT00673855 | Acute Comfort of Lubricant Eye Drops FID 112903 | COMPLETED | NA | 2008-05 | 2008-05 | 2008-05 |
| NCT00763360 | To Compare the Ability of DiscoVisc® OVD to Protect the Corneal Endothelium and Maintain Anterior Chamber Space With Healon® and Amvisc® PLUS During Cataract Surgery. | COMPLETED | PHASE4 | 2008-05 | | 2010-09 |
| NCT00762216 | Rotational Stability of the AcrySof® Toric | COMPLETED | NA | 2008-05 | | 2009-06 |
| NCT00691665 | Comparison of Olopatadine 0.6% and Fluticasone Proprionate 50mcg Nasal Sprays in a Two Week Seasonal Allergic Rhinitis Trial | COMPLETED | PHASE4 | 2008-05 | | 2009-01 |
| NCT00705770 | A Multi-Dose Study With a Treatment for Open-Angle Glaucoma | WITHDRAWN | PHASE2, PHASE3 | 2008-05 | 2008-07 | 2008-07 |
| NCT00670033 | Travoprost New Formulations in Patients With Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE2 | 2008-04 | 2008-09 | 2008-09 |
| NCT00724412 | Evaluate Artificial Tear Efficacy in Moderate to Severe Dry Eye | COMPLETED | PHASE4 | 2008-04 | 2009-02 | 2009-02 |
| NCT00691457 | Comparison of 3 Novel Contact Lens Solutions on the Basal Lamina | COMPLETED | NA | 2008-04 | 2009-01 | 2009-01 |
| NCT00725530 | Evaluation of Deposits on Contact Lenses Worn Extended Wear | COMPLETED | NA | 2008-03 | 2008-10 | 2008-10 |
| NCT00725153 | Evaluation of Deposits on Contact Lenses Worn Daily Wear | COMPLETED | NA | 2008-03 | 2008-09 | 2008-09 |
| NCT00643669 | 24 Hour IOP Lowering Efficacy of AL-3789 | COMPLETED | PHASE2 | 2008-02 | | 2008-04 |
| NCT00758576 | ReSTOR Natural +3.0D Study In Japan | COMPLETED | NA | 2008-02 | 2009-12 | 2009-12 |
| NCT00631358 | Assessment of Inflammatory Biomarkers Expressed in a Sjogren's Population: Effect of a Topical Steroid Intervention | COMPLETED | PHASE4 | 2008-02 | | 2009-02 |
| NCT00733291 | Evaluation of Daily Disposable Lenses With Multi-Purpose Solution (MPS) | COMPLETED | NA | 2008-01 | 2008-02 | 2008-02 |
| NCT00576342 | Patient Preference Study | COMPLETED | PHASE3 | 2007-12 | 2008-01 | 2008-01 |
| NCT00579020 | A Phase II Study of Moxidex Ophthalmic Solution for Treatment of Marginal Corneal Infiltrates | TERMINATED | PHASE2 | 2007-12 | 2009-02 | 2009-02 |
| NCT00673959 | Acute Comfort of Lubricant Eye Drop FID 111421 | COMPLETED | NA | 2007-12 | | 2008-02 |
| NCT00620256 | Adjunctive Study of AL-37807 Ophthalmic Suspension | COMPLETED | PHASE2 | 2007-11 | 2008-07 | 2008-07 |
| NCT00578773 | A Phase II Study of an Otic Formulation in Treating Peri-Operative Tube Otorrhea | COMPLETED | PHASE2 | 2007-11 | 2009-01 | 2009-01 |
| NCT00568386 | Acute Comfort and Blur of Systane and Optive | COMPLETED | NA | 2007-11 | 2007-12 | |
| NCT00934622 | Visual Function After Implantation of Bilateral AcrySoft ReSTOR Aspheric IOL | COMPLETED | PHASE4 | 2007-11 | | 2009-03 |
| NCT00637130 | Safety and Intraocular Pressure (IOP) Lowering Efficacy of Low Dose Travoprost | COMPLETED | PHASE2 | 2007-10 | | 2008-01 |
| NCT00759941 | A Comparison of Azopt Versus Placebo Added to Xalatan in Patients With Elevated Intraocular Pressure (IOP) on a Prostaglandin | COMPLETED | PHASE4 | 2007-10 | 2009-07 | 2009-07 |
| NCT00508469 | Adherence Assessment With Travalert Dosing Aid | COMPLETED | PHASE4 | 2007-10 | 2010-01 | 2010-01 |
| NCT00712244 | DisCoVisc Versus DuoVisc, Healon5 and AmVisc Plus | COMPLETED | PHASE4 | 2007-10 | | 2009-04 |
| NCT00576251 | TOBRADEX Ophthalmic Suspension Versus Tobramycin 0.3%/Dexamethasone 0.05% Ophthalmic Suspension | COMPLETED | PHASE3 | 2007-10 | 2008-03 | 2008-02 |
| NCT00713076 | Wettability of Contact Lenses With a Multi-Purpose Solution | COMPLETED | NA | 2007-10 | | 2008-03 |
| NCT00532415 | Safety and Efficacy of Vitreous Delineating Agent During Vitrectomy | COMPLETED | PHASE3 | 2007-09 | 2007-09 | 2007-09 |
| NCT00719732 | Visual Function After Implantation of Bilateral AcrySof ReSTOR Aspheric +3 | COMPLETED | PHASE4 | 2007-09 | 2009-05 | 2009-05 |
| NCT00578929 | Safety and Efficacy of Olopatadine HCl Nasal Spray in 6-11 Year Old Patients | COMPLETED | PHASE3 | 2007-09 | | 2008-11 |
| NCT00519753 | Success of Transitioning Uncontrolled Glaucoma Patients From Prior Mono or Adjunctive Therapy to DuoTrav | COMPLETED | PHASE4 | 2007-08 | 2008-12 | 2008-12 |
| NCT00527501 | IOP Lowering Efficacy of Travoprost/Brinzolamide Fixed Combination Ophthalmic Suspension in Patients With Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE2 | 2007-08 | 2007-12 | 2007-12 |
| NCT00721253 | Visual Outcomes of Subjects Bilaterally Implanted With ReSTOR Aspheric +4 vs. Tecnis or Acri.LISA | COMPLETED | PHASE4 | 2007-07 | 2008-10 | 2008-10 |
| NCT00711347 | Intraoperative Floppy Iris Syndrome | COMPLETED | PHASE4 | 2007-06 | 2008-04 | 2008-04 |
| NCT00684138 | ACRYSOF® ReSTOR® Aspheric +3.0 D Add Power Intraocular Lens (IOL) | COMPLETED | PHASE4 | 2007-06 | 2008-06 | 2008-06 |
| NCT00731640 | Contralateral ReSTOR / Monofocal or Phakic Eye | COMPLETED | PHASE4 | 2007-06 | | 2008-05 |
| NCT00732030 | Low Cylinder Toric | COMPLETED | PHASE4 | 2007-06 | | 2009-03 |
| NCT00527592 | A Single Dose Comfort Comparison of Travatan Z in One Eye Versus Xalatan in the Opposite Eye in Patients With Primary Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE4 | 2007-05 | 2008-08 | 2008-08 |
| NCT00468988 | Short Term Comparative Study of Xalatan With Benzalkonium Chloride vs. Travatan Z Without Benzalkonium Chloride in Healthy Volunteers | COMPLETED | PHASE4 | 2007-05 | 2007-07 | 2007-07 |
| NCT00759668 | Visual Function and Patient Satisfaction After Bilateral Implantation of AcrySof Natural ReSTOR (Model SN60D3) or AcrySof Natural Monofocal (Model SN60AT) | COMPLETED | NA | 2007-05 | 2009-09 | 2009-09 |
| NCT00732225 | DisCoVisc Comparative Evaluation | COMPLETED | PHASE3 | 2007-05 | | 2008-02 |
| NCT00759096 | Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL | COMPLETED | NA | 2007-05 | 2008-07 | 2008-07 |
| NCT00444665 | Examining The Efficacy, Safety And Improved Tolerability Of Travoprost BAK Free Ophthalmic Solution (Travatan-Z) Compared To Prior Prostaglandin Therapy | COMPLETED | PHASE4 | 2007-05 | 2007-08 | 2007-08 |
| NCT00758550 | Visual Function After Bilateral Implantation of AcrySof® Toric | COMPLETED | PHASE4 | 2007-04 | | 2008-06 |
| NCT00451152 | Safety and Efficacy of Anecortave Acetate in Patients With Open-Angle Glaucoma | COMPLETED | PHASE2 | 2007-03 | 2009-07 | 2009-07 |
| NCT00465803 | A Phase IIIb Study of DuoTrav to Treat Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2007-03 | | 2009-01 |
| NCT00471380 | A Phase IV Study of Travoprost + Brinzolamide to Treat Glaucoma or Ocular Hypertension | COMPLETED | PHASE4 | 2007-03 | | 2008-10 |
| NCT00471068 | Study of Travatan and Cosopt in Primary Open-Angle Glaucoma or Ocular Hypertension | TERMINATED | PHASE4 | 2007-03 | | 2008-08 |
| NCT00465621 | Dose Response Study of AL-37807 Ophthalmic Solution in Patients With Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE2 | 2007-03 | | 2007-07 |
| NCT00762645 | Travoprost 0.004% Versus Pilocarpine 1% in Patients With Chronic Angle Closure Glaucoma (CACG) | COMPLETED | PHASE4 | 2007-02 | 2008-05 | 2008-05 |
| NCT00051129 | Anecortave Acetate in Subfoveal Choroidal Neovascularization (CNV) Due to Wet Age-Related Macular Degeneration (AMD) | COMPLETED | PHASE3 | 2007-01 | 2008-05 | 2008-05 |
| NCT00762021 | Posterior Capsule Opacification (PCO) Evaluation of the AcrySof SN60AT Lens vs. SN60WF Lens | COMPLETED | NA | 2006-12 | | 2009-08 |
| NCT00578331 | Safety Study of Olopatadine Nasal Spray | COMPLETED | PHASE3 | 2006-12 | 2008-01 | 2008-01 |
| NCT00404937 | Tobradex BID Compared to TOBRADEX and TOBREX/Vehicle | WITHDRAWN | PHASE3 | 2006-12 | 2006-12 | 2006-12 |
| NCT00473070 | A Clinical Study of Tobradex AF | COMPLETED | PHASE3 | 2006-11 | | 2007-02 |
| NCT00760487 | Visual Function After Implantation of Bilateral AcrySof® Toric Natural Intraocular Lens | COMPLETED | PHASE4 | 2006-10 | | 2008-06 |
| NCT00389025 | Mast-Cell Stabilizing Effects of Olopatadine | COMPLETED | PHASE4 | 2006-10 | | 2007-04 |
| NCT00332657 | Anecortave Acetate Risk Reduction Trial (AART) | TERMINATED | PHASE3 | 2006-09 | 2008-12 | 2008-12 |
| NCT00300079 | Study of the Intraocular Pressure (IOP)-Lowering Efficacy of Azopt 1.0% Compared to Timolol 0.5% in Patients With Glaucoma or Ocular Hypertension | COMPLETED | PHASE4 | 2006-09 | 2007-09 | 2007-09 |
| NCT00382226 | IOP-Lowering Efficacy of Brinzolamide 1.0% Added to Travoprost 0.004%/Timolol 0.5% Fixed Combination as Adjunctive Therapy | COMPLETED | PHASE4 | 2006-09 | 2007-08 | 2007-08 |
| NCT00346528 | Safety of NGOIS Compared to BSS Plus in Pediatric Patients | COMPLETED | PHASE3 | 2006-07 | 2007-06 | 2007-06 |
| NCT00348517 | Safety/Efficacy of Systane Free vs Refresh Liquigel | COMPLETED | NA | 2006-07 | 2006-11 | 2006-11 |
| NCT00348322 | Safety/Efficacy of Systane Free vs Refresh Tears | COMPLETED | NA | 2006-07 | 2006-11 | 2006-11 |
| NCT00471419 | Phase II Study of AL-2178 (FID 109980) in the Treatment of Dry Eye | COMPLETED | PHASE3 | 2006-07 | 2007-08 | 2007-08 |
| NCT00312338 | Topical Treatment of Bacterial Conjunctivitis and Its Effect on Microbial Flora | COMPLETED | PHASE4 | 2006-06 | 2007-06 | 2007-06 |
| NCT00332293 | AL-15469A for the Treatment of Bacterial Conjunctivitis | COMPLETED | PHASE3 | 2006-05 | 2006-12 | 2006-12 |
| NCT00763061 | Travatan Versus Timoptic in Treating Open-angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE4 | 2006-05 | 2008-04 | 2008-04 |
| NCT00758342 | Azopt (Brinzolamide 1.0%) Plus Travatan (Travoprost 0.004%) in Treating Patients With Chronic Angle-Closure Glaucoma (CACG) | TERMINATED | PHASE4 | 2006-05 | 2008-03 | 2008-03 |
| NCT00372931 | A Phase II Study of AL-37807 to Treat Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE2 | 2006-05 | | 2007-08 |
| NCT00326092 | A Study of a Glaucoma Therapy to Treat Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE2 | 2006-05 | 2006-08 | 2006-08 |
| NCT00331500 | Olopatadine 0.2% for the Treatment of Allergic Conjunctivitis | COMPLETED | PHASE3 | 2006-04-18 | 2006-07-27 | 2006-07-27 |
| NCT00333125 | A Study of Glaucoma Therapy to Treat Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2006-04 | 2007-02 | 2007-02 |
| NCT00362895 | A Bioequivalence Study of Tobradex AF | COMPLETED | PHASE3 | 2006-04 | 2006-08 | 2006-08 |
| NCT00347854 | Fluorophotometry Evaluation of Lubricant Eye Drops | COMPLETED | NA | 2006-04 | 2006-04 | 2006-04 |
| NCT00320203 | Anecortave Acetate in Patients With Open-angle Glaucoma | COMPLETED | PHASE2 | 2006-03 | 2008-01 | 2008-01 |
| NCT00330798 | A Comparison of Topical Nepafenac to Placebo in Corneal Epithelial Healing Times and Postoperative Pain Relief | COMPLETED | PHASE4 | 2006-02 | 2006-06 | 2006-06 |
| NCT00332774 | Nevanac 3-Month Safety Study With QID Dosing | COMPLETED | PHASE3 | 2006-02 | 2006-12 | 2006-12 |
| NCT00579189 | Phase III Study of an Otic Formulation in Acute Otitis Media With Tympanostomy Tubes | COMPLETED | PHASE3 | 2006-01 | 2009-01 | 2009-01 |
| NCT00293761 | A Study of Glaucoma Therapy to Treat Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2006-01 | 2006-05 | 2006-05 |
| NCT00758745 | Randomized Contralateral Clinical Trial With Single-piece (SN60WF) vs. Three Piece (MA60AC) AcrySof Intraocular Lenses (IOLs) on Development of Posterior Chamber Opacification (PCO). | COMPLETED | NA | 2006-01 | 2009-12 | 2009-12 |
| NCT00051168 | A Long-term Safety Study of Once-daily Travatan | COMPLETED | PHASE3 | 2006-01 | | 2009-03 |
| NCT00578474 | A Phase III Study of an Otic Formulation in Acute Otitis Media With Tympanostomy Tubes | COMPLETED | PHASE3 | 2005-12 | 2008-08 | 2008-08 |
| NCT00315640 | Anecortave Acetate for Treatment of Steroid Induced Intraocular Pressure (IOP) Elevation | COMPLETED | PHASE2 | 2005-12 | 2009-07 | 2009-07 |
| NCT00347984 | Product Preference With Systane Compared to Artificial Tears on Frequency of Drop Use | COMPLETED | NA | 2005-12 | 2006-02 | 2006-02 |
| NCT00405730 | Nepafenac 0.1% Eye Drops, Suspension Compared to Ketorolac Trometamol 0.5% Eye Drops, Solution and Placebo | COMPLETED | PHASE3 | 2005-11 | 2006-07 | 2006-07 |
| NCT00287521 | A Study of Glaucoma Therapy to Treat Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE2 | 2005-11 | 2006-02 | 2006-02 |
| NCT00314158 | A Study of a Glaucoma Therapy to Treat Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2005-11 | 2007-01 | 2007-01 |
| NCT00331916 | AL-15469A for the Treatment of Bacterial Conjunctivitis | COMPLETED | PHASE3 | 2005-11 | | 2007-05 |
| NCT00333203 | Next Generation Ophthalmic Irrigating Solution Posterior Segment Study | COMPLETED | PHASE3 | 2005-10 | 2006-03 | 2006-03 |
| NCT00314171 | A Study of a Glaucoma Therapy to Treat Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2005-10 | 2007-08 | 2007-08 |
| NCT00333255 | Nepafenac Opthalmic Suspension 0.1% Compared to Acular LS for Treatment of Inflammation After Cataract Surgery | COMPLETED | PHASE3 | 2005-09 | | 2006-03 |
| NCT00333216 | Anecortave Acetate Risk-Reduction Trial (AART) | TERMINATED | PHASE3 | 2005-05 | 2008-12 | 2008-12 |
| NCT00299507 | Anecortave Acetate in Patients With Exudative Age-related Macular Degeneration (AMD) | COMPLETED | PHASE3 | 2005-03 | 2008-04 | 2008-04 |
| NCT00383201 | Effect of Multi-Purpose Solutions on Ex-Vivo Wetting Angles | COMPLETED | NA | 2005-03 | 2005-09 | 2005-09 |
| NCT00288951 | Phase III Safety and Efficacy Study to Evaluate a Glaucoma Therapy in Open-Angle Glaucoma or Ocular Hypertension Patients | COMPLETED | PHASE3 | 2004-10 | 2005-06 | 2005-06 |
| NCT00333268 | Safety and Efficacy of Next Generation Ophthalmic Irrigating Solution Compared to BSS Plus | COMPLETED | PHASE3 | 2004-09 | 2005-07 | 2005-07 |
| NCT00382902 | Evaluation of an Investigational Multi-Purpose Disinfecting Solution for the Care of Silicone Hydrogel Soft Contact Lenses | COMPLETED | NA | 2004-08 | 2005-02 | 2005-02 |
| NCT00382603 | Evaluation of an Investigational Multi-Purpose Disinfecting Solution for the Care of Soft Contact Lenses in Symptomatic Patients | COMPLETED | NA | 2004-08 | 2005-02 | 2005-02 |
| NCT00293800 | A Study of Glaucoma Therapy to Treat Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2004-07 | 2005-12 | 2005-12 |
| NCT00382681 | Evaluation of an Investigational Multi-Purpose Disinfecting Solution for Care of Soft Contact Lenses | COMPLETED | NA | 2004-07 | 2004-11 | 2004-11 |
| NCT00293787 | A Study of Glaucoma Therapy to Treat Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2004-06 | 2005-08 | 2005-08 |
| NCT00307398 | Anecortave Acetate Risk-Reduction Trial (AART) | TERMINATED | PHASE3 | 2004-03 | 2009-01 | 2009-01 |
| NCT00372827 | Study of Brinzolamide and Timolol When Added to Travoprost in Primary Open-angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE4 | 2004-02 | 2006-01 | 2006-01 |
| NCT00069706 | Phase II Safety and Efficacy Study to Evaluate a Glaucoma Therapy in Open-angle Glaucoma or Ocular Hypertension Patients | COMPLETED | PHASE2 | 2003-07 | 2003-10 | 2003-10 |
| NCT00065728 | Open-Label Posterior Juxtascleral Injections of Anecortave Acetate 15mg Dose for Long Term Use in Patients With AMD | TERMINATED | PHASE3 | 2003-06 | 2008-10 | 2008-10 |
| NCT00061503 | Mechanism of Action of TRAVATAN 0.004% in Subjects With Glaucoma or Ocular Hypertension | COMPLETED | PHASE4 | 2003-04 | 2004-03 | 2004-03 |
| NCT00058994 | An Evaluation of Safety and Efficacy of Anecortave Acetate Versus Placebo in Patients With Subfoveal CNV Due to Exudative AMD | COMPLETED | PHASE3 | 2003-03 | 2006-11 | 2006-11 |
| NCT00311389 | A 12-Month Study to Evaluate the Efficacy and Safety of Once-Daily Instillation of Combination Glaucoma Therapy in Patients With Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2003-01 | 2004-09 | 2004-09 |
| NCT00061516 | Safety and Efficacy Study of BETAXON 0.5% and AZOPT 1.0% in Pediatric Patients With Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2003-01 | 2006-02 | 2006-02 |
| NCT00061529 | A Phase III Study of Brimonidine Tartrate Ophthalmic Solution, 0.15% in Patients With Open-Angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2003-01 | 2004-07 | 2004-07 |
| NCT00061542 | Safety and Efficacy Study of BETOPTIC S 0.25% and Timolol Gel-forming Solution 0.25% and 0.5% in Pediatric Patients With Glaucoma or Ocular Hypertension | COMPLETED | PHASE3 | 2003-01 | 2006-11 | 2006-11 |
| NCT00051194 | A 6-week Safety & Efficacy Study of Combination Intraocular Pressure-lowering Therapy in Patients With Open-angle Glaucoma or Ocular Hypertension | COMPLETED | PHASE2 | 2002-09 | 2003-07 | 2003-07 |
| NCT00047606 | Phase 4 Study Comparing IOP Lowering in OAG or OH in Caucasian or Japanese Subjects C-02-32 | TERMINATED | PHASE4 | 2002-08 | 2003-11 | 2003-11 |
| NCT00041483 | Phase 3 Study to Evaluate Anecortave Acetate vs. Visudyne for the Treatment of the Wet Form of AMD | COMPLETED | PHASE3 | 2002-06 | 2005-08 | 2005-08 |
| NCT00051142 | A Safety and Efficacy Study of Travoprost 0.004% Compared to Latanoprost 0.005% in Patients With Open-Angle Glaucoma (OAG) or Ocular Hypertension (OHT) | COMPLETED | PHASE3 | 2001-02 | 2004-06 | 2004-06 |
| NCT00047541 | Phase 3 Study to Evaluate IOP Lowering Therapy in Open Angle Glaucoma and Ocular Hypertension C-01-70 | COMPLETED | PHASE3 | 2001-02 | 2003-11 | 2003-11 |
| NCT00047528 | Phase 3 Study to Evaluate IOP Lowering Therapy in Open Angle Glaucoma and Ocular Hypertension C-02-41 | COMPLETED | PHASE3 | 2001-01 | 2003-11 | 2003-11 |
| NCT00047515 | Phase 3 Study to Evaluate IOP Lowering Therapy in Open Angle Glaucoma and Ocular Hypertension C-01-69 | COMPLETED | PHASE3 | 2001-01 | 2003-12 | 2003-12 |
| NCT00051155 | A 6-Week Safety and Efficacy Study of Travatan Compared to Xalcom in Subjects With Open-Angle Glaucoma(OAG) or Ocular Hypertension(OHT) | COMPLETED | PHASE3 | 2001-01 | 2004-07 | 2004-07 |
| NCT00346866 | Anecortave Acetate Versus Placebo in AMD Patients Following PDT | COMPLETED | PHASE2 | 2000-05 | 2001-12 | 2001-12 |
| NCT00047593 | Phase 3 Study Comparing IOP Lowering in OAG or OH in Japanese Subjects C-01-98 | COMPLETED | PHASE3 | 2000-01 | 2004-07 | 2004-07 |
| NCT00051181 | A Safety and Efficacy Study of Travoprost 0.004% Compared to Latanoprost 0.005% in Patients With Chronic Angle-Closure Glaucoma | COMPLETED | PHASE3 | 2000-01 | 2003-06 | 2003-06 |
| NCT00346957 | A Phase II Study of Anecortave Acetate for the Treatment of Exudative Age-Related Macular Degeneration | COMPLETED | PHASE2 | 1999-04 | 2003-04 | 2003-04 |
| NCT00069719 | Phase II Safety and Efficacy Study to Evaluate a Glaucoma Therapy in Open-Angle Glaucoma or Ocular Hypertension Patients | COMPLETED | PHASE2 | 1999-02 | 2003-08 | 2003-08 |
| NCT00758940 | Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL | WITHDRAWN | PHASE4 | | | |
| NCT00761488 | Recommendations for Monitoring Clinical Experience Following Implantation of the AcrySof® Toric | WITHDRAWN | PHASE4 | | | |