Smith & Nephew, Inc.: all 214 studies

Page 1 of 3. Open to participants first (12), then studies with results posted, then the rest; newest registration first within each.

• Sacrum Pressure Injury Prevention Study Using ALLEVYN◊ Complete Care in Adults at Risk of Developing Hospital-acquired Pressure Injuries in Critical Care UnitsNot yet recruitingNCT07849387Not applicable
• Knee Cartilage Repair RegistryRecruitingNCT07786207
• A Multi-Center Study Assessing the Safety and Efficacy of the LEGION Medial Stabilized (MS) Insert in Patients Undergoing a Total Knee Arthroplasty (TKA)RecruitingNCT07199738
• Post-Market Clinical Study to Evaluate the Safety and Effectiveness of REFLEX ULTRA 45 for Coblation Inferior Turbinate Reduction in ChinaRecruitingNCT07025304Not applicable
• A Post Approval Multicenter 10 Year Follow-up Observational Trial of Marketed Product - MP01 vs. Surgical Standard of Care (SSOC) Used for the Treatment of Joint Surface Lesions of the KneeEnrolling by invitationNCT06916728
• Clinical Trial on the Effect of the Flexible Suturing System With Anchors (FSSA) in Full-thickness Rotator Cuff Tendon TearsEnrolling by invitationNCT06868108
• Evaluation Of Outcomes Following Rotator Cuff Repair Using the REGENETEN Bioinductive ImplantRecruitingNCT06857084
• AETOS Shoulder SystemRecruitingNCT06319911
• Evaluation of Outcomes Following In-office Tympanostomy Using the Tula® System: a Prospective, Multi-center RegistryRecruitingNCT05915078
• Use of the REGENETEN™ Bioinductive Implant System in High Grade Partial-thickness TearsRecruitingNCT05444465Not applicable
• Study to Evaluate the Safety and Effectiveness of the REAL INTELLIGENCE™ CORI™ in Total Knee Arthroplasty (TKA) ProcedureRecruitingNCT04848896Not applicable
• A Multicenter, Post-Market Clinical Follow-up Study of Subjects With the REDAPT™ System Monolithic Sleeveless/Sleeved Stem and/or Fully Porous Acetabular Shell With XLPE Liner and/or Modular Shell Components Previously ImplantedEnrolling by invitationNCT03610789
• Human Participant Study of a Prototype Multilayer Foam Dressing on Intact Skin.CompletedNCT06831448Not applicableResults posted
• Human Participant Study of Prototype Non-medicated Multilayer Foam Dressings on Intact SkinCompletedNCT06700850Not applicableResults posted
• Study to Evaluate the PICO 14 Negative Pressure Wound Therapy System in the Management of Acute and Chronic WoundsTerminatedNCT05234632Results posted
• Study to Evaluate the Safety and Efficacy of OR3O™ Dual Mobility System vs. Conventional Single Bearing Design Total Hip SystemTerminatedNCT04941729Not applicableResults posted
• Safety and Performance Study of the FAST-FIX FLEX System for Meniscal Repairs and Meniscal TransplantationsCompletedNCT04903106Results posted
• To Evaluate the Performance of the CORI™ KNEE TENSIONER as an Accessory to the CORI™ Surgical System.CompletedNCT04849884Not applicableResults posted
• Evaluate the Performance of JOURNEY II CR in TKA PopulationsTerminatedNCT04818840Results posted
• Study to Evaluate the Safety and Effectiveness of REAL INTELLIGENCE™ CORI™ in Unicondylar Knee Arthroplasty (UKA) ProceduresTerminatedNCT04797897Not applicableResults posted
• Study to Evaluate the Safety and Effectiveness of REAL INTELLIGENCE™ CORI™ in Knee Arthroplasty ProceduresCompletedNCT04786119Not applicableResults posted
• Safety of Treatment of Shoulder RepairCompletedNCT04552119Results posted
• REGENETEN™ Bioinductive Implant System in Full-thickness TearsTerminatedNCT04450342Not applicableResults posted
• EU Safety and Efficacy Study Regarding the R3 Acetabular Hip SystemCompletedNCT04399928Results posted
• Safety and Performance of ENTACT Septal Staple System for SeptoplastyCompletedNCT04392583Results posted
• Circumferential Compression STITCH Repairs of Complex and Horizontal Cleavage Meniscal TearsTerminatedNCT04361487Results posted
• A Study of the Safety and Performance of the MINITAC◊ Titanium 2.0 Suture AnchorCompletedNCT04186481Results posted
• Performance, Safety and Efficacy of NPWT DeviceCompletedNCT04102865Not applicableResults posted
• LEGION™ Primary Safety and EfficacyTerminatedNCT04040985Not applicableResults posted
• Safety and Effectiveness of BIOSURE RG in Cruciate Ligaments Reconstruction in ChineseCompletedNCT04012567Not applicableResults posted
• Safety and Performance of MICRORAPTOR™ Suture Anchors in Shoulder and HipCompletedNCT03985839Results posted
• Evaluation of the Safety and Effectiveness of ALLEVYN Gentle BorderCompletedNCT03877484Results posted
• PMCF Study on PEEK Suture Anchors for Shoulder IndicationsCompletedNCT03826667Results posted
• PMCF Study on PEEK Suture Anchors for Hip IndicationsCompletedNCT03814044Results posted
• Safety and Performance of PEEK Anchors in ExtremitiesCompletedNCT03782298Results posted
• Treatment of Partial-Thickness Rotator Cuff TearsTerminatedNCT03734536Not applicableResults posted
• Safety Study of Femoral Neck Fracture SystemTerminatedNCT03721835Not applicableResults posted
• Safety and Performance of the SUTUREFIX ULTRA and SUTUREFIX CURVED Suture Anchors in Shoulder and Hip Arthroscopic RepairCompletedNCT03691298Results posted
• A Safety Follow Up Study in Australian Subjects Implanted With the SMF Short Modular Femoral Stem Hip SystemTerminatedNCT03646513Results posted
• S&P of Q-Fix™ All-Suture Anchor SystemCompletedNCT03594071Results posted
• Post-Approval Study of the R3 Biolox Delta Ceramic Acetabular System - EuropeCompletedNCT03566082Results posted
• In-Office Tympanostomy Tube Placement in Children (OTTER)CompletedNCT03323736Phase 3Results posted
• Navio With Total Knee ArthroplastyCompletedNCT03317834Results posted
• Agili-C™ Implant Performance EvaluationCompletedNCT03299959Not applicableResults posted
• Long Term Follow-up of Integra® Cadence™ Total Ankle System in Primary Ankle Joint ReplacementTerminatedNCT03247023Results posted
• Adult Study to Evaluate Placement of Tympanostomy Tubes In-office (ADEPT)CompletedNCT03197558Phase 2Results posted
• Evaluation Of An Advanced Borderless DressingCompletedNCT03146845Not applicableResults posted
• Study to Compare Active Tymbion Iontophoresis to Sham Tymbion Iontophoresis for Anesthesia of the Tympanic MembraneCompletedNCT03119181Phase 2Results posted
• A Retrospective Study of the Navio Robotic-assisted Surgical SystemCompletedNCT03072459Results posted
• R3 Delta Ceramic Acetabular System PAS U.S.CompletedNCT03056534Results posted
• PyroTITAN Humeral Resurfacing Arthroplasty (HRA)CompletedNCT02983292Results posted
• Achilles Tendon Repair With Bioinductive ImplantCompletedNCT02811003Not applicableResults posted
• Study of SANTYL® vs Hydrogel (SoloSite®) for Pressure UlcersTerminatedNCT02718625Phase 4Results posted
• Intraoperative Case Series Study: Trial Rasp Position Versus SL-PLUS™ MIA Ti/HA Femoral Hip Stem PositionCompletedNCT02664272Results posted
• POLARSTEM Cementless Hip StemCompletedNCT02648152Results posted
• Use of Santyl in Diabetic Foot UlcersCompletedNCT02581488Phase 4Results posted
• Single-Use Negative Pressure Wound Therapy System vs. Traditional Negative Pressure Wound Therapy System (tNPWT)CompletedNCT02470806Not applicableResults posted
• Ascension® Post- Approval Study; PyroCarbon Metacarpophalangeal Total Joint ProsthesisTerminatedNCT02408471Not applicableResults posted
• A Multi-center Outcomes Clinical Study of the PyroTITAN™ HRA Shoulder Implant in Humeral Head ResurfacingCompletedNCT02405208Results posted
• OXINIUM◊ DH Total Hip Arthroplasty Pivotal StudyActive, not recruitingNCT02353377Results posted
• Multicenter Clinical Observation PROMOS®CompletedNCT02280499Results posted
• Study of Suture Repair of Torn Meniscus in the KneeCompletedNCT02237001Not applicableResults posted
• Post-Market Evaluation of the Rotation Medical Rotator Cuff SystemCompletedNCT02200939Not applicableResults posted
• A RCT to Compare the Effects of Two Wound Products on Biofilm Disruption in DFUsTerminatedNCT02181621Not applicableResults posted
• Pilot Study Evaluating the Safety and Efficacy of a New Hard-on-Hard Total Hip Replacement SystemCompletedNCT02154516Not applicableResults posted
• A Phase 2 Exploratory Pharmacodynamic Study of HP802-247 in Venous Leg UlcersTerminatedNCT02154087Phase 2Results posted
• A Pilot Study to Assess the DynaSense SystemCompletedNCT02005692Not applicableResults posted
• A Pilot Study of the WoundWand™ Debridement Device on Infection PreventionTerminatedNCT01924806Not applicableResults posted
• Safety and Efficacy Trial of HP802-247 in the Treatment of Chronic Venous Leg UlcersTerminatedNCT01853384Phase 3Results posted
• Study of Oasis Ultra in Diabetic Foot UlcersCompletedNCT01835379Phase 4Results posted
• Mechanical vs. Radiofrequency-Based Debridement in the Treatment of Articular Cartilage LesionsTerminatedNCT01803880Not applicableResults posted
• Study Investigating the Safety and Efficacy of HP802-247 in the Treatment of Venous Leg Ulcers >12 cm2 to ≤ 36 cm2CompletedNCT01737762Phase 3Results posted
• Study Investigating the Safety and Efficacy of HP802-247 in the Treatment of Venous Leg UlcersCompletedNCT01656889Phase 3Results posted
• PICO Breast Reduction Clinical Study Looking at Incision Healing ComplicationsCompletedNCT01640366Not applicableResults posted
• Comparison of HP011-101 to Standard Care for Stage I-II Pressure Ulcers in Subjects With Spinal Cord InjuryTerminatedNCT01433159Phase 2Results posted
• Using Santyl on Diabetic Foot UlcersCompletedNCT01408277Phase 4Results posted
• Healing Effects of HP802-247 Versus Antibiotic Ointment in Mohs Micrographic Surgery PatientsCompletedNCT01359735Phase 2Results posted
• TRIGEN SURESHOT™ Distal Targeting System StudyTerminatedNCT01327508Not applicableResults posted
• Study to Determine if Fibrin Affects the Ability of a Wound to HealCompletedNCT01253135Phase 1Results posted
• Wound Edge Changes Following Treatment With SantylCompletedNCT01197898Phase 4Results posted
• Study of Survival Duration for Donor Skin Cells in Skin Biopsy WoundsCompletedNCT01190865Phase 1Results posted
• Enzymatic Versus (vs) Autolytic Debridement of Diabetic Foot UlcersCompletedNCT01143727Phase 4Results posted
• A Study to Look at the Effects of Four Weeks of Treatment on the Healing of Diabetic Foot UlcersCompletedNCT01143714Phase 4Results posted
• Evaluation of Effects of HP828-101 for Moisture Associated Skin DamageTerminatedNCT01108523Early Phase 1Results posted
• Visionaire™ Versus Standard Instrumentation Safety and Efficacy in Total Knee Arthroplasty (TKA)TerminatedNCT01084772Not applicableResults posted
• Mini Stem DEXA (Dual Energy X-ray Absorptiometry)CompletedNCT01066936Results posted
• Mini Stem Radiostereometric Analysis StudyCompletedNCT01064531Results posted
• Santyl vs. Sharp Debridement of Diabetic Foot WoundsCompletedNCT01056198Phase 4Results posted
• Trial of Versajet Compared With Conventional Treatment in Acute and Chronic WoundsCompletedNCT01050673Not applicableResults posted
• Evaluation of the Use of EZCare/V1STA in the Management of Acute and Chronic WoundsCompletedNCT00994162Not applicableResults posted
• Evaluation of the Effects of HP828-101 Versus Standard of Care in the Management of Partial or Full Thickness WoundsCompletedNCT00971048Not applicableResults posted
• Safety Follow-Up to HP 802-247-09-015CompletedNCT00900029Results posted
• Dose Finding Study of HP802-247 in Venous Leg UlcersCompletedNCT00852995Phase 2Results posted
• Contact Sensitization Potential of 828 OintmentCompletedNCT00767676Phase 1Results posted
• Cumulative Irritation Potential of 828 OintmentCompletedNCT00767455Phase 1Results posted
• Study of the ENTact Septal Staple System for Tissue Approximation During SeptoplastyCompletedNCT00740480Results posted
• Controlled Study of the Effect of Xenaderm® Ointment Vehicle Versus White Petrolatum on HealingCompletedNCT00713349Phase 2Results posted
• Safety and Effectiveness Study of the Reflection Ceramic Acetabular SystemCompletedNCT00663351Not applicableResults posted
• Effect of Collagenase on Healing and ScarringCompletedNCT00651820Phase 4Results posted
• Clinical Evaluation of the Photoallergy Potential of Xenaderm OintmentCompletedNCT00645164Phase 1Results posted

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