Smith & Nephew, Inc.: all 214 studies
Page 2 of 3. Open to participants first (12), then studies with results posted, then the rest; newest registration first within each.
- Clinical Evaluation of the Phototoxic Potential of Xenaderm OintmentCompletedNCT00644917Phase 1Results posted
- OASIS Wound Matrix (Oasis) Mechanism of ActionCompletedNCT00570141Phase 4Results posted
- A Multi-Centre Study in Patients Undergoing Total Hip Arthroplasty With the Smith+Nephew CATALYSTEM™ Primary Hip SystemActive, not recruitingNCT06564636
- PICO Venous Leg Ulcers (VLU) Reimbursement StudyTerminatedNCT06510777Not applicable
- A Clinical Study on New Negative Pressure Wound Therapy Dressing in the Management of Chronic & Acute WoundsTerminatedNCT06306716
- Study to Evaluate Patient Outcomes and Safety and Effectiveness of Robotic Assisted Unicompartmental Knee Replacements Versus Conventional Unicompartmental Knee for Subjects With Primary Arthritis of the Knee Joint Involving One (UKA) Compartment (Medial or Lateral)WithdrawnNCT06036212Not applicable
- A Global Clinical Study Investigating the Safety and Effectiveness of Smith and Nephew's Porous Knee System in Patients Who Need a Total Knee Replacement Due to Degenerative Arthritis, Post-traumatic Arthritis or Inflammatory ArthritisActive, not recruitingNCT05197036
- A Comparison of Patients Receiving a Unicompartmental Knee Replacement With Robotic Assistance or With Conventional InstrumentationWithdrawnNCT04992078Not applicable
- Patient Outcomes Using HIP7 Software as Compared to Conventional THAWithdrawnNCT04989998Not applicable
- A Comparison of Patients Receiving a Total Knee Replacement With Robotic Assistance or With Conventional InstrumentationWithdrawnNCT04976972Not applicable
- A Study to Evaluate the Safety and Effectiveness of TRIGEN™ INTERTAN™ (10S Models)WithdrawnNCT04865146
- Evaluate the Performance of JOURNEY II CR and JOURNEY II BCS in TKA PopulationsWithdrawnNCT04822259Not applicable
- Anthology Hip Replacement System - Orthopaedic Data Evolution Panel (ODEP) Surveillance StudyCompletedNCT04425603
- Safety and Effectiveness Study of OR3O™ Dual Mobility System in THAActive, not recruitingNCT04325022
- Retro-prospective Study of Safety & Performance of Round XTENDOBUTTON™ Fixation Device Post Knee RepairCompletedNCT04211857
- Assessment of Implant Fixation and SF-36 for Short Hip-Stems - A Prospective Clinical StudyCompletedNCT04172129
- Prospective Single-center Long-term Observation of the SL-PLUS® MIA StemCompletedNCT04122157
- Clinical Observation Study of the Hydroxylapatite-coated SL-PLUS™ Hip ShaftTerminatedNCT04121585
- NANOS Neck Preserving Hip StemTerminatedNCT04036279
- Clinical Observation Study of the Hydroxylapatite-coated SLPLUS™MIA Hip ShaftTerminatedNCT04036071
- Five and Ten Year Results of the CMK21 Hip SystemTerminatedNCT03908151
- Safety and Performance of Journey II BCS Total Knee System Patient Reported Outcome MeasuresCompletedNCT03903731
- Safety and Efficacy of the ANTHEM™ CR Total Knee SystemActive, not recruitingNCT03885622
- Safety and Performance of JOURNEY™ II Cruciate Retaining (CR) Total Knee System (TKS)CompletedNCT03885531
- Safety Study of Treatment of Leg FracturesTerminatedNCT03881241
- A Clinical Study to Assess the Safety and Clinical Performance of a New Dressing (PICO7Y) in Breast Surgery PatientsCompletedNCT03835845Not applicable
- Safety and Performance of Journey II XR Total Knee SystemCompletedNCT03798847
- Safety and Performance of the Journey™ II UNI Unicompartmental Knee SystemCompletedNCT03768128
- A Clinical Study to Evaluate the Safety and Efficacy of Q-Fix Trial in Chinese PatientsCompletedNCT03765515Not applicable
- Safety and Performance of the TFCC FastFix in the WristCompletedNCT03756714
- Safety and Performance Study of the Legion Porous System in Total Knee ArthroplastyActive, not recruitingNCT03720782
- Performance, Safety and Efficacy of PICO Device.CompletedNCT03698968Not applicable
- Safety and Performance Using Legion™ CR Oxinium and CoCr Femoral Implants Combined With Legion™/Genesis™ II XLPE High Flex Tibial InsertsActive, not recruitingNCT03687593
- Study to Evaluate Safety and Efficacy of GrafixPL for the Treatment of Venous Leg UlcersCompletedNCT03629236Not applicable
- BIOSURE™ RG Knee Safety & Performance StudyCompletedNCT03519555
- Journey™ UNI Post Market Clinical Follow-UpActive, not recruitingNCT03442231
- Non-Comparative Study of Open Abdomen That Require the Use of Negative Pressure Wound Therapy (NPWT) for Temporary Abdominal ClosureWithdrawnNCT03431220Not applicable
- Journey II Bi-Cruciate Stabilized (BCS) Total Knee System Retrospective StudyCompletedNCT03292003
- DURAFIBER Ag Post-Market Clinical Follow-UpCompletedNCT03277131Not applicable
- Clinical Evaluation of the Integra® Titan™ Modular Shoulder System Generation 2.5 for Primary Shoulder Joint ReplacementTerminatedNCT03250767
- Clinical Evaluation of the TITAN™ Total Shoulder SystemTerminatedNCT03245320
- Clinical Evaluation of Integra® Cadence™ Total Ankle System in Primary Ankle Joint Replacement (CADENCE)SuspendedNCT03142958
- JOURNEY II XR Safety and Effectiveness PMCFActive, not recruitingNCT03136887
- Predictors of Early Success From Circumferential Compression STITCH Meniscal RepairsCompletedNCT03097744
- Ten Year Implant Survivorship of the ANTHEM™ PS Total Knee SystemActive, not recruitingNCT03078543
- Trigen InterTAN vs Sliding Hip Screw RCTTerminatedNCT03065101Not applicable
- TruSkin®: Study for Treatment of Chronic Venous Leg UlcersTerminatedNCT02936128Phase 4
- TruSkin®: Study for the Treatment of Chronic Diabetic Foot UlcersTerminatedNCT02936115Phase 4
- Comparison of Surgical Incision Complications in Patients Receiving PICO or Standard Care Following Colorectal SurgeryWithdrawnNCT02883010Not applicable
- ACTICOAT™ for the Treatment of Burns and Chronic WoundsCompletedNCT02852148Not applicable
- Agili-CTM Implant Performance Evaluation in the Treatment of Osteoarthritis of the Great ToeCompletedNCT02831244Not applicable
- Journey II BCS CMS Total Knee System Compared to Other PS Total Knee Systems in PT SettingTerminatedNCT02820766
- Treatment of Wounds With a New Adhesive Foam DressingCompletedNCT02807584Not applicable
- Rotation Medical Bioinductive Implant Database RegistryCompletedNCT02784600
- Managing Wounds With Allevyn Life in a Home Health Care EnvironmentWithdrawnNCT02776800Not applicable
- Use of Santyl Within an Accountable Care OrganizationWithdrawnNCT02716519Phase 4
- POLARSTEM Retrospective Multicenter StudyCompletedNCT02680340
- GrafixPRIME® for the Treatment of Chronic Diabetic Foot UlcersCompletedNCT02675855Phase 4
- REDAPT Retrospective-Prospective Modular Stem StudyTerminatedNCT02661620
- Study to Evaluate the Safety and Efficacy of CHAM* for the Treatment of Diabetic Foot UlcersTerminatedNCT02571738Phase 3
- The Clinical Efficacy of RENASYS TOUCH NPWT System in the Management of Acute, Sub-acute and Chronic WoundsCompletedNCT02565043Not applicable
- Clinical Outcome Following Total Hip Arthroplasty With the SMF StemTerminatedNCT02471703
- Trial of PICO Versus Standard Care in Chronic and Sub-acute WoundsTerminatedNCT02458859Not applicable
- LEGION Hinge Safety and Efficacy StudyActive, not recruitingNCT02445443
- JOURNEY™ II CR Total Knee SystemActive, not recruitingNCT02440672
- A Retro-prospective Study of Total Hip Arthroplasty With EMPERION Modular Primary Stem in Australian Centres (HISTORIC)TerminatedNCT02435420
- Agili-C™ Implant Performance Evaluation in the Repair of Cartilage and Osteochondral DefectsCompletedNCT02423629Not applicable
- LEGION™ Revision Metal Hypersensitivity StudyWithdrawnNCT02412813Not applicable
- Ascension PyroCarbon Radial Head StudyTerminatedNCT02405234Not applicable
- BIOSURE™ HEALICOIL™ PK Bone In-growth StudyCompletedNCT02382341
- Post Market Clinical Follow Up of LEGION™ Primary TKS With VERILAST™Active, not recruitingNCT02380092
- Project JAY HAP Registration StudyCompletedNCT02347397Not applicable
- Project JAY THA Registration StudyCompletedNCT02347384Not applicable
- REDAPT Revision System Study to Assess 5 Year Revision Rate & up to 10 Year Revision Rate and Safety and EffectivenessWithdrawnNCT02344160
- Clinical Observation Study With the SBG StemCompletedNCT02338661
- GrafixCORE®: Open-Label Study to Evaluate the Safety and Efficacy of GrafixCORE® for Complex Diabetic Foot WoundsCompletedNCT02260609Phase 4
- Journey II BCS EU Observational TrialActive, not recruitingNCT02211794
- TITAN™ Reverse Shoulder SystemTerminatedNCT02204228
- Visionaire Health Economics Study Comparing Economic Outcomes Between Visionaire and Standard InstrumentationCompletedNCT02158819Not applicable
- TC-A Registration StudyCompletedNCT02139345Not applicable
- Santyl Applications to Diabetic Foot UlcersCompletedNCT02111291Phase 4
- A RCT to Compare Performance of Two Foam Dressings on Patient Well-being Related Endpoints.CompletedNCT02053337Not applicable
- Observational Study Providing 12 Months of Safety Follow-Up From First Exposure to HP802-247CompletedNCT01970657
- Pilot Study of the Use of ULTRABRAID PLUS SUTURE in the Repair of Tears of the Rotator CuffCompletedNCT01767740Not applicable
- A Prospective, Randomized, Multi-Center Evaluation of MediENT® Middle Turbinate Implant Versus MeroPack®, a Bioresorbable Nasal Dressing / Sinus Stent After Endoscopic Sinus SurgeryCompletedNCT01733667Not applicable
- Long Term Follow Up to Determine the Effects of Collagenase SANTYL Ointment on Scar FormationCompletedNCT01705860
- Safety and Efficacy of the Journey II BCS Total Knee SystemCompletedNCT01705067
- A Study of Patients Treated With the Journey Deuce Bicompartmental Knee SystemCompletedNCT01704326
- Safety Study Providing 12 Months Follow-up From First Exposure to HP802-247 in Subjects With Venous Leg UlcerStatus unknownNCT01658618
- Grafix® DFU: Open-Label Extension Option to Evaluate Safety & Efficacy of Grafix® for Chronic Diabetic Foot UlcersCompletedNCT01596920Phase 4
- OPSITE Post-Op Visible Wound Dressings in Treatment of Surgical IncisionsCompletedNCT01577225Not applicable
- Research Study to Compare the Addition of Topaz Micro Debridement to the Standard of Care SurgeryCompletedNCT01562366Not applicable
- A Pilot Study of HP802-247 in Dystrophic Epidermolysis BullosaWithdrawnNCT01528306Phase 2
- Using Santyl or Bacitracin on Second Degree BurnsWithdrawnNCT01516463Phase 4
- Evaluation of the Agili-C Biphasic Implant in the Knee JointCompletedNCT01471236Not applicable
- Safety and Efficacy of the SL PLUS and the SL PLUS MIA Hip StemCompletedNCT01435850Phase 4
- Clinical Outcome of Birmingham Hip Resurfacing (BHR) Using VISIONAIRE Femoral Alignment GuideCompletedNCT01427361
- R3® Acetabular System in Patients With Degenerative Hip DiseaseCompletedNCT01407029
- Efficacy Study of Surgical Technique in Intramedullary Tibia Nailing, Using Trigen META Tibia NailsCompletedNCT01358292Phase 4
- HP011-101, HP828-101, and Standard Care for Pressure UlcersWithdrawnNCT01273428Phase 2