| NCT06937216 | Evaluation of the Effectiveness of The Volara System Determined by Sputum Movement and Production | NOT_YET_RECRUITING | NA | 2025-05 | 2025-11 | 2025-09 |
| NCT06842134 | A Study Comparing Organic Phosphate (Sodium Glycerophosphate Injection) to Numeta G16%E | COMPLETED | PHASE1 | 2025-01-27 | 2025-05-22 | 2025-05-22 |
| NCT06842121 | A Bioequivalence Study Comparing Organic Phosphate (Sodium Glycerophosphate Injection) to Inorganic Phosphate (Sodium Phosphates Injection, USP) | COMPLETED | PHASE1 | 2025-01-27 | 2025-05-22 | 2025-05-22 |
| NCT05976425 | ModPG3 Neo-Infant ISO 81060 | RECRUITING | NA | 2024-02-23 | 2025-08 | 2025-05 |
| NCT06056011 | Timmy3 Module Clinical Accuracy ISO 80601-2-56:2017 + A1 2018 | ENROLLING_BY_INVITATION | NA | 2024-02-19 | 2025-09-30 | 2025-05-30 |
| NCT05567601 | Doxil/Caelyx BE Study | COMPLETED | PHASE1 | 2023-12-16 | 2024-06-21 | 2024-06-21 |
| NCT05647161 | BAX602 in Preventing the Adhesion Around Great Cardiac Vessels in Pediatric Patients With Congenital Heart Disease Undergoing Re-do Open Heart Surgery (Japan Trial) | ACTIVE_NOT_RECRUITING | NA | 2022-12-08 | 2025-12-31 | 2025-10-31 |
| NCT05309304 | Cefazolin PK Study 3g vs 2g | COMPLETED | PHASE1 | 2022-02-14 | 2022-08-30 | 2022-08-30 |
| NCT05366010 | Oscillation and Lung Expansion (OLE) Therapy for Treatment of Neuromuscular Disease (NMD) Patients | TERMINATED | NA | 2021-11-04 | 2024-02-27 | 2024-02-27 |
| NCT06894446 | Efficacy and Safety of Numeta G13%E Compared to Compounded Parenteral Nutrition in Preterm Neonates | WITHDRAWN | PHASE3 | 2021-08-20 | 2022-05-30 | 2022-05-30 |
| NCT04555044 | Pediatric Study to Evaluate Risk of Developing Essential Fatty Acid Deficiency When Receiving Clinolipid or Standard-of-Care Lipid Emulsion (Part A) | COMPLETED | PHASE4 | 2021-01-22 | 2022-11-16 | 2022-10-16 |
| NCT04324593 | Healthy Volunteer Study to Evaluate the Impact of Various Common Interventions on Venous Pressure Signal Captured by PIVA | TERMINATED | NA | 2020-02-26 | 2020-03-21 | 2020-03-21 |
| NCT04155814 | Bioequivalence Study Assessing Iron Sucrose or VenoferĀ® in Healthy Adult Subjects | COMPLETED | PHASE1 | 2019-09-19 | 2019-12-18 | 2019-12-18 |
| NCT04017312 | A Pilot Study to Evaluate the Use of the VestĀ® System for Treatment of Bronchiectasis Patients in the Home Setting | TERMINATED | NA | 2019-08-23 | 2024-08-06 | 2024-08-06 |
| NCT04083807 | Efficacy and Safety of TISSEEL Lyo Compared to Manual Compression as an Adjunct to Haemostasis | COMPLETED | PHASE3 | 2019-07-10 | 2019-10-22 | 2019-10-22 |
| NCT03450265 | Hemopatch Compared to TachoSil in Postoperative Air Leak Duration After Pulmonary Resection | COMPLETED | NA | 2018-06-26 | 2019-07-09 | 2019-07-09 |
| NCT03797677 | MN4000 for Treatment of CF and MND Patients in the Home Setting | COMPLETED | NA | 2017-03-09 | 2017-11-30 | 2017-11-30 |
| NCT02891070 | Efficacy and Safety of FS VH S/D 500 S-apr (Tisseel) as an Adjunct to Sutured Dural Repair in Cranial Surgery | COMPLETED | PHASE3 | 2016-10-11 | 2018-08-22 | 2018-08-22 |
| NCT02837731 | Fluid Responsiveness Evaluation in Sepsis-associated Hypotension | COMPLETED | NA | 2016-10 | 2019-03-13 | 2019-03 |
| NCT02871258 | MetaNebĀ® Chest X-ray Study | COMPLETED | NA | 2016-09 | 2017-08-17 | 2017-08-17 |
| NCT02627742 | Evaluation of The MetaNebĀ® System to Reduce Postoperative Pulmonary Complications | COMPLETED | NA | 2016-03 | 2017-08 | 2017-08 |
| NCT02640235 | Effectiveness and Safety of CELSTAT for Hemostasis in Intraoperative Tissue Bleeding | COMPLETED | NA | 2016-02-24 | 2017-10-18 | 2017-07-21 |
| NCT02476994 | Pediatric Study to Evaluate Risk of Developing Essential Fatty Acid Deficiency When Receiving Clinolipid or Standard-of-Care Lipid Emulsion | TERMINATED | PHASE4 | 2015-05 | 2016-10 | 2016-10 |
| NCT01923480 | Dosing Study of Amino Acids in Seriously Ill Patients | TERMINATED | PHASE4 | 2013-07 | 2014-12 | 2014-12 |
| NCT01637025 | Oxidized Cellulose hEmostAsis evaluatioN | COMPLETED | NA | 2012-05 | 2012-11 | 2012-11 |
| NCT01579097 | Comparative Phase 3 Trial to Assess the Safety and Efficacy of Triple-chamber Parenteral Nutrition Formulation | COMPLETED | PHASE3 | 2011-12 | 2013-01 | 2012-11 |
| NCT01484106 | Cardiac Output Monitoring Managing Intravenous Therapy (COMMIT) to Treat Emergency Department Severe Sepsis | COMPLETED | NA | 2011-11 | 2014-08 | 2014-08 |
| NCT01452022 | Performance of Inductigraft in Spinal Fusion | COMPLETED | NA | 2011-10 | 2015-08 | 2015-08 |
| NCT01410240 | Efficacy and Safety of FLOSEAL for Hemostasis in Total Knee Arthroplasty | COMPLETED | PHASE4 | 2011-09 | 2013-01 | 2013-01 |
| NCT01234883 | Intravenous (IV) Solutions for Dehydration in Children With Gastroenteritis | TERMINATED | PHASE4 | 2011-06 | 2013-02 | 2013-02 |
| NCT01413074 | Survival on Peritoneal Dialysis (PD) Versus Hemodialysis (HD) in China | TERMINATED | PHASE4 | 2011-06 | 2013-12 | 2013-12 |
| NCT01244425 | Fibrin Sealant VH S/D 500 S-apr in Hepatic Resection | COMPLETED | PHASE2 | 2010-11 | 2011-07 | 2011-07 |
| NCT01112735 | Efficacy and Safety of ARTISS for Flap Adherence in Abdominoplasty | COMPLETED | PHASE2 | 2010-05 | 2011-02 | 2010-12 |
| NCT01120431 | Efficacy and Time and Resources for Hylenex-facilitated SC Rehydration Versus ORT for Dehydrated Children in the Emergency Department (ED) | WITHDRAWN | PHASE4 | 2010-05 | 2010-05 | 2010-05 |
| NCT01116102 | Study of In-line Pressure Using Various Techniques of Subcutaneous Administration of Fluids Enabled by Human Recombinant Hyaluronidase (INFUSE-AT1A) | TERMINATED | PHASE4 | 2010-05 | 2010-06 | 2010-05 |
| NCT00999141 | Efficacy and Safety of FS VH S/D 4 S-apr for Flap Adherence in Rhytidectomy | COMPLETED | PHASE3 | 2009-09 | 2010-02 | 2009-12 |
| NCT01018771 | Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion | COMPLETED | NA | 2009-07 | 2012-12 | 2012-12 |
| NCT00892957 | FS VH S/D 500 S-apr in Vascular Surgery | COMPLETED | PHASE3 | 2009-07 | 2010-11 | 2010-10 |
| NCT00957255 | Rotator Cuff Repair (RCR) With and Without OrthoADAPT Augmentation | WITHDRAWN | NA | 2009-03 | 2010-04 | 2010-04 |
| NCT00953563 | The Mechanism of Action of Unite Biomatrix in Venous Leg Ulcers | WITHDRAWN | NA | 2009-03 | 2011-07 | 2011-07 |
| NCT00958711 | The Mechanism of Action of the Unite Biomatrix in Diabetic Foot Ulcer | TERMINATED | NA | 2009-01 | 2012-05 | 2012-05 |
| NCT00807885 | Study of Techniques of Subcutaneous Administration of Fluids Enabled by Human Recombinant Hyaluronidase | COMPLETED | PHASE4 | 2008-12 | 2009-01 | 2009-01 |
| NCT00771238 | Pilot Study of Incidence and Change in Existing Pressure Ulcers: TC500 Bed Compared With Standard Beds | COMPLETED | NA | 2008-11 | 2010-01 | 2010-01 |
| NCT00739193 | A Randomized, Placebo-Controlled, Double-Blind, Double Dummy Trial To Determine The Relative Effect Of Pm101 Versus Placebo And Amiodarone IV On Blood Pressure In Subjects With Stable Congestive Heart Failure | WITHDRAWN | PHASE2 | 2008-08 | 2008-12 | 2008-12 |
| NCT00962143 | Acute Achilles Repair With or Without OrthADAPT Augmentation | WITHDRAWN | NA | 2008-06 | 2011-01 | 2010-12 |
| NCT00708071 | Efficacy and Safety Study of Fibrin Sealant With 4 IU/mL Thrombin, Vapor Heated, Solvent Detergent Treated (FS VH S/D 4) in Face-Lift Procedures | COMPLETED | PHASE2 | 2008-06 | 2008-09 | 2008-09 |
| NCT00681824 | Fibrin Sealant for the Sealing of Dura Sutures | COMPLETED | PHASE2 | 2008-05 | 2010-03 | 2010-03 |
| NCT00762372 | Japan Phase 2/3 Clinical Study With BLM-240 (Desflurane) | COMPLETED | PHASE2, PHASE3 | 2008-02 | 2008-08 | 2008-08 |
| NCT01304394 | Safety During Use of Paediatric Triple Chamber Bag Formulas | COMPLETED | PHASE3 | 2008-02 | 2009-06 | 2008-12 |
| NCT00576420 | Fibrin Sealant Vascular Surgery Study | COMPLETED | PHASE2 | 2007-12 | 2008-12 | 2008-11 |
| NCT00477152 | Study of Subcutaneous Rehydration With Recombinant Human Hyaluronidase for Infants and Children | COMPLETED | PHASE4 | 2007-08 | 2008-06 | 2008-06 |
| NCT00508495 | Analgesic Efficacy, Safety and Tolerability of Two Paracetamol-Containing Solutions in Post-Surgical Hip Replacement Pain | COMPLETED | PHASE3 | 2007-08 | 2008-03 | 2008-03 |
| NCT00502346 | A Trial to Determine the Relative Effect of PM101 I.V. Versus Placebo on Hemodynamics in Healthy Adult Volunteers | COMPLETED | PHASE1 | 2007-07-03 | 2007-11-02 | 2007-11-02 |
| NCT00510549 | Comparison of the Impact of Dialysis Treatment Type on Patient Survival | COMPLETED | PHASE4 | 2007-07 | 2008-08 | 2008-08 |
| NCT01013389 | Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion (PLIF) With Interbody Fusion | COMPLETED | NA | 2007-06 | 2012-12 | 2012-12 |
| NCT00493220 | Pharmacokinetic and Safety Study of HYLENEX Recombinant-Augmented Subcutaneous Ceftriaxone Administration | COMPLETED | PHASE1 | 2007-06 | 2007-09 | 2007-09 |
| NCT00559013 | Peri-Strips Dry (PSD) Veritas Collagen Matrix Staple Line Reinforcement for Colorectal Surgery | COMPLETED | NA | 2007-03 | 2008-12 | 2008-12 |
| NCT00420953 | Relative Bioavailability of PM101 IV and Cordarone IV | COMPLETED | PHASE1 | 2006-12-18 | 2007-04-23 | 2007-04-23 |
| NCT00406679 | Analgesic Efficacy, Safety and Tolerability of Two Paracetamol-containing Solutions in Post-Surgical Dental Pain | COMPLETED | PHASE3 | 2006-11 | 2007-10 | 2007-10 |
| NCT00566943 | Reinforcement of Surgical Staple Lines Using Peri-Strips Dry (PSD) With Veritas Collagen Matrix | COMPLETED | NA | 2006-03 | 2008-12 | 2008-12 |
| NCT00163605 | Performance and Safety of Bone Substitute MBCP-FS in Maxillary Sinus Lift Procedures | COMPLETED | PHASE2, PHASE3 | 2004-09 | 2007-11 | |
| NCT00157131 | Safety and Efficacy Study of FS 4 IU VH S/D (Fibrin Sealant With 4IU/mL Thrombin, Vapor Heated, Solvent/Detergent Treated) to Adhere Split Thickness Skin Grafts and Improve Wound Healing in Burn Patients | COMPLETED | PHASE3 | 2004-06 | 2007-02 | 2007-02 |
| NCT00161733 | Safety and Hemostatic Efficacy of Fibrin Sealant Vapor Heated, Solvent/Detergent Treated (FS VH S/D) Compared With Currently Licensed TISSEEL VH Fibrin Sealant in Subjects Undergoing Cardiac Surgery | COMPLETED | PHASE3 | 2002-09 | 2004-11 | |
| NCT00161759 | Safety and Efficacy Study of Fibrin Sealant (FS 4IU) for Skin Graft Fixation and Wound Healing in Subjects With Burn Wounds | COMPLETED | PHASE1, PHASE2 | 2002-03 | 2004-01 | |
| NCT00161902 | Efficacy and Safety of Fibrin Sealant Vapor Heated Solvent/Detergent Treated (FS VH S/D) for Hemostasis in Subjects Undergoing Total Hip Replacement | COMPLETED | PHASE3 | 2001-08 | 2003-03 | |
| NCT00161980 | Efficacy and Safety of Fibrin Sealant Vapor Heated Solvent/Detergent Treated (FS VH S/D) for Reduction of Lymphatic Leakage by Sealing Axillary Lymph Node Dissection Sites | COMPLETED | PHASE3 | 2001-06 | 2002-12 | |
| NCT00512356 | Efficacy and Safety Study of Anti-Adhesion Product in the Prevention of Intraperitoneal Adhesions | COMPLETED | PHASE2 | 2000-12 | 2003-04 | 2003-02-25 |
| NCT00161915 | Efficacy and Safety of Endoscopic Injection of Fibrin Sealant Versus Endoscopic Ligature for Bleeding Esophageal Varices | COMPLETED | PHASE3 | 2000-12 | 2004-01 | |
| NCT00358553 | A Crossover Study Assessing the Pharmacokinetics, Pharmacodynamics, and Safety of Recombinant Human Insulin | COMPLETED | PHASE1 | | | |