Integra LifeSciences Corporation: all 92 studies

Page 1 of 1. Open to participants first (5), then studies with results posted, then the rest; newest registration first within each.

• Urinary Bladder Matrix (UBM) RegistryNot yet recruitingNCT07805798
• AERA Pediatrics RegistryRecruitingNCT07071298
• A Modified Platform Trial of Multiple CAMPs for the Management of Diabetic Foot Ulcers and Venous Leg UlcersEnrolling by invitationNCT06453187Not applicable
• Bactiseal Catheter Safety Registry StudyRecruitingNCT06276543
• The MIRROR Registry: Minimally Invasive IntRaceRebral HemORrhage EvacuationRecruitingNCT04494295
• T-GENVIH-003 LTFU (Long Term Follow Up) StudyCompletedNCT06034652Results posted
• External Ventricular Drainage Post-Market Clinical Follow-up RegistryCompletedNCT05652296Results posted
• Gentrix® Surgical Matrix for Soft Tissue Reinforcement in Ventral Hernia RepairCompletedNCT05610267Results posted
• Bactiseal Catheter Safety Registry in ChinaCompletedNCT04496414Results posted
• A Study on the Safety of Hakim Programmable Shunt SystemCompletedNCT04285489Results posted
• The Management of Pilonidal Wounds With ACell MicroMatrix® and Cytal® Wound Matrix: A Case SeriesTerminatedNCT04041037Results posted
• Sundt™ Carotid Shunt Retrospective Post Market Clinical Follow-up Study (PMCF)CompletedNCT03816202Results posted
• Cytal® Wound Matrix and MicroMatrix® Wound StudyTerminatedNCT03632954Results posted
• Diabetic Foot Ulcer Study Comparing Cytal Wound Matrix 1-Layer to Standard of CareTerminatedNCT03626623Not applicableResults posted
• AMNIOEXCEL® Plus vs A Marketed Comparator vs SOC in the Management of Diabetic Foot UlcersCompletedNCT03547635Not applicableResults posted
• Comparing Concomitant Use of ACell MicroMatrix® and ACell Cytal™ to Standard of Care in Stage 3 or 4 Pressure InjuriesCompletedNCT03283787Not applicableResults posted
• PriMatrix for the Management of Diabetic Foot UlcersCompletedNCT03010319Not applicableResults posted
• Global Sinus Surgery RegistryTerminatedNCT02347943Results posted
• Duragen® Secure Post Marketing Clinical Follow-up (PMCF)CompletedNCT02225080Results posted
• Acclarent Tympanostomy Tube Delivery System for the Treatment of Patients Requiring Tympanostomy Tube InsertionCompletedNCT02150044Not applicableResults posted
• Study of Safety and Efficacy for the Eustachian Tube Balloon CatheterCompletedNCT02087150Not applicableResults posted
• A Comparative Efficacy Study: Treatment for Non-healing Diabetic Foot UlcersTerminatedNCT01858545Not applicableResults posted
• Comparison of Balloon Sinuplasty In-Office Versus Medical Management for Recurrent Acute Sinusitis Patients (CABERNET)CompletedNCT01714687Not applicableResults posted
• Medical Therapy Versus Balloon Sinus Dilation for Patients With Chronic RhinosinusitisCompletedNCT01685229Results posted
• Tympanostomy Tube Placement in Children in the Office (Inova Study)CompletedNCT01496287Not applicableResults posted
• inVENT-visIOn StudyCompletedNCT01444391Not applicableResults posted
• inVENT-In-Office StudyCompletedNCT01324271Not applicableResults posted
• Evaluation of the Tympanostomy Tube Delivery SystemCompletedNCT01202578Phase 2/3Results posted
• Optimization and Refinement of Technique in In-Office Sinus Dilation 2CompletedNCT01107379Results posted
• A Safety and Efficacy Study of INTEGRA® Dermal Regeneration Template for the Treatment of Diabetic Foot UlcersCompletedNCT01060670Not applicableResults posted
• Clinical Evaluation of the Ethmoid Sinus SpacerTerminatedNCT01054703Not applicableResults posted
• Singapore Tympanostomy Tube Delivery System StudyCompletedNCT01046877Not applicableResults posted
• An Evaluation of SprayShield in Reducing Post-Operative Adhesion Formation Following Major Open Abdominal SurgeryTerminatedNCT01002287Not applicableResults posted
• Anesthetic Effect of Lidocaine/Epinephrine Solution Delivered Via Iontophoresis to External Auditory ApparatusCompletedNCT00941993Not applicableResults posted
• Clinical Study of the Tympanostomy Tube Delivery SystemCompletedNCT00939796Not applicableResults posted
• Safety and Efficacy of Balloon Sinuplasty in Pediatric SinusitisCompletedNCT00939471Not applicableResults posted
• Balloon Sinus Dilation In Office or ORCompletedNCT00939393Not applicableResults posted
• Post Market Study for an Adhesion Barrier Following Laparoscopic MyomectomyCompletedNCT00891657Not applicableResults posted
• Clinical Study of Safety and Efficacy for the Relieva Stratus With Elution of Triamcinolone AcetonideCompletedNCT00791934Not applicableResults posted
• DuraSeal Sealant Post Market StudyCompletedNCT00704340Not applicableResults posted
• PleuraSeal Post Market Study (Europe)CompletedNCT00704171Phase 4Results posted
• Study to Evaluate Safety and Effectiveness of Spinal SealantCompletedNCT00594035Not applicableResults posted
• Study to Evaluate Safety & Effectiveness of Spinal SealantCompletedNCT00444067Not applicableResults posted
• Study to Evaluate Safety & Effectiveness of Vascular Sealant SystemTerminatedNCT00439309Not applicableResults posted
• DuraGen Plus® Adhesion Barrier for Use in Spinal SurgeryTerminatedNCT00387829Not applicableResults posted
• Clinical Evaluation to Confirm Safety and Efficacy of Sinuplasty in the Paranasal Sinuses (CLEAR)CompletedNCT00231062Phase 3Results posted
• Tissue Quality of Integra vs. BTM Treated BurnsWithdrawnNCT06760611
• MicroMatrix® Flex in Tunneling WoundsCompletedNCT06629506Not applicable
• Cavitronic Ultrasonic Surgical Aspiration (CUSA) Women's Health StudyCompletedNCT06297187
• Post Market Clinical Follow-up of CODMAN CERTAS Programmable ValveActive, not recruitingNCT05397106
• NeuraGen 3D Pilot StudyTerminatedNCT05343143Not applicable
• REINVENT Registry (Registry of the Nerve Gap Repair From Integra)TerminatedNCT05339594
• The SurgiMend PRS Retrospective StudyCompletedNCT05182177
• The Purpose of This Study is to Determine Whether CerebroFlo™ EVD Catheter is Effective During the Treatment of Intraventricular Hemorrhage (IVH)CompletedNCT05113381Not applicable
• AmnioExcel® Plus vs SOC in the Management of Diabetic Foot UlcersWithdrawnNCT05024656Not applicable
• Suturable DuraGen™ PMCF StudyCompletedNCT04923867
• DuraSorb® in Prosthetic Breast ReconstructionActive, not recruitingNCT04646057Not applicable
• The CUSA Clarity Bone Tip StudyWithdrawnNCT04300075
• The CUSA Clarity Soft Tissue Removal StudyCompletedNCT04298268
• CERTAS Programmable Valve RegistryCompletedNCT04207229
• A Study to Evaluate the Efficacy of Cytal® Burn Matrix in the Management of Partial-Thickness Burns to the HandWithdrawnNCT03598023Not applicable
• MEDIHONEY® Gel Versus Collagenase for Wound DebridementTerminatedNCT02482948Not applicable
• Ascension® Humeral Resurfacing Arthroplasty (HRA) Follow-Up StudyTerminatedNCT02369497
• Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot UlcersCompletedNCT02209051Not applicable
• Observational Study of Total Ankle Arthroplasty and Tibiotalar ArthrodesisWithdrawnNCT02025946
• ACell MatriStem Pelvic Floor Matrix Versus Native Tissue Repair, Comparative StudyCompletedNCT02021279Not applicable
• SurgiMend in Two-stage Implant-based Breast Reconstruction in Patients With Pre-Mastectomy RadiotherapyWithdrawnNCT01959867Not applicable
• Retrospective Study Evaluating Outcomes for Integra® Skin Sheet Products in Lower Extremity Complex WoundsCompletedNCT01947387
• Phase 3 Study Evaluating Efficacy and Safety of DSC127 Compared With Vehicle and With Standard-of-care in Diabetic Foot UlcersTerminatedNCT01849965Phase 3
• Open-Label Study in Diabetic Foot Ulcers (DFU), to Evaluate Safety of 0.03% DSC127 Topical Gel in Chronic UseTerminatedNCT01840085Phase 3
• Phase III Study to Evaluate Efficacy and Safety of DSC127 in Diabetic Foot UlcersTerminatedNCT01830348Phase 3
• Prospective, Multicenter Observational Study Evaluating the Long Term Safety of the Custombone ImplantCompletedNCT01824706
• Health Economic Assessment of Lower Extremity Diabetic (HEALED) Ulcers With PriMatrixTerminatedNCT01729286Not applicable
• Clinical Outcome of Defect Reconstruction Using IDRT Single Layer : Results From a Prospective Multicentric TrialCompletedNCT01704950
• A Multi-center, Prospective, Randomized Study With PriMatrix and PriMatrix Ag for the Treatment of Venous Leg UlcersTerminatedNCT01612806Not applicable
• Earset Healthy Volunteer StudyCompletedNCT01611246
• Follow-up of Patient Implanted With the Staple ASTUS®TerminatedNCT01518543
• Canadian Health Economics, Outcome, and Effectiveness Comparison of Treatment in Patients With Chronic RhinosinusitisTerminatedNCT01455948Not applicable
• DuraSeal Exact Spine Sealant System Post-Approval StudyCompletedNCT01410864
• Healthy Volunteer StudyCompletedNCT01346332
• Evaluation of Integra® Artificial Dermis for the Treatment of Leg UlcersCompletedNCT01285973
• Short Term Follow-up of Patient Implanted With the Proximal Interphalangeal ImplantCompletedNCT01285011
• Short Term Follow-up of Patent Implanted With the B-BOP Lock PlateCompletedNCT01284998
• Short Term Follow-up of Patient Implanted With the Metatarso-Phalangeal Prosthesis METIS®CompletedNCT01284985
• HINTEGRA Total Ankle Prosthesis Follow-upCompletedNCT01284972
• A Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot UlcersTerminatedNCT01270633Not applicable
• A Multicenter, Prospective, Observational Study With PriMatrix for the Treatment of Neuropathic Diabetic Foot UlcersCompletedNCT01228526
• The Use of Bioscaffolds in Conjunction With Negative Pressure Therapy: A Prospective Randomized Double-Blinded TrialWithdrawnNCT01228500Not applicable
• Anesthetizing the Tympanic Membrane in Healthy VolunteersCompletedNCT01047904Not applicable
• Large Abdominal Hernia Repair With SurgiMend 3.0CompletedNCT00892333
• PleuraSeal Pivotal Study (US)TerminatedNCT00748124Phase 3
• Stabilization of Trochanteric Fracture Using a Screw-plate TRAUMAXCompletedNCT00703716

← Integra LifeSciences Corporation overview and focus areas