Edwards Lifesciences: all 141 studies

Page 1 of 2. Open to participants first (22), then studies with results posted, then the rest; newest registration first within each.

• The CLASP III TR CED StudyNot yet recruitingNCT07859709
• Early Feasibility Study of the Edwards APTURE Transcatheter Shunt SystemRecruitingNCT07858799Not applicable
• CLAARITY is a Prospective, Observational, Single-arm, Multi-center, Post-market US Study Designed to Evaluate the Safety and Performance of the ECLIPTIS Left Atrial Appendage Exclusion System for Exclusion of the Left Atrial Appendage (LAA) During Concomitant Open-heart Cardiac Surgery.Not yet recruitingNCT07742839
• TRIFORMIS RESILIA Real-world Study Assessing Safety and Performance (TRIBLAZE Study)RecruitingNCT07684313
• KONECT RESILIA Aortic Valved Conduit (AVC) Real-world Study Assessing Safety and PerformanceRecruitingNCT07619872
• JOURNEY LVAD: JOURNEY Left Ventricular Assist DeviceNot yet recruitingNCT07363473Not applicable
• Real World Data Collection on the INSPIRIS RESILIA Aortic ValveRecruitingNCT07120048
• MITRIS China Post Market Clinical Follow-up (PMCF) StudyRecruitingNCT07059793
• TTVR STRONG Under Coverage With Evidence Development (CED) StudyRecruitingNCT06833476
• Real World Effectiveness of the Cordella Pulmonary Artery Sensor System in Patients With Chronic Heart Heart FailureRecruitingNCT06783335
• Real World European Investigation of Safety and Clinical Efficacy of the EVOQUE System (TRISCEND III EU)RecruitingNCT06569602
• J-Valve Transfemoral Pivotal StudyRecruitingNCT06455787Not applicable
• ALLIANCE Mitral: Safety and Effectiveness of SAPIEN X4 Transcatheter Heart Valve - MitralNot yet recruitingNCT06167213Not applicable
• PROACTIVE-HF-2 Trial Heart Failure NYHA Class II and IIIRecruitingNCT05934487Not applicable
• ALLIANCE AVIV: Safety and Effectiveness of the SAPIEN X4 Transcatheter Heart Valve in Failing Aortic Bioprosthetic ValvesRecruitingNCT05172973Not applicable
• ALLIANCE: Safety and Effectiveness of the SAPIEN X4 Transcatheter Heart ValveRecruitingNCT05172960Not applicable
• TVMR With the INNOVALVE System Trial - Early Feasibility StudyRecruitingNCT04919980Not applicable
• PROGRESS: Management of Moderate Aortic Stenosis by Clinical Surveillance or TAVRRecruitingNCT04889872Not applicable
• Edwards PASCAL Transcatheter Valve Repair System Pivotal Clinical TrialRecruitingNCT04097145Not applicable
• Early Feasibility Study - Edwards APTURE Transcatheter Shunt SystemRecruitingNCT03523416Not applicable
• PARTNER 3 Trial - Aortic Valve-in-ValveRecruitingNCT03003299Not applicable
• COMPASSION S3 - Evaluation of the SAPIEN 3 Transcatheter Heart Valve in Patients With Pulmonary Valve DysfunctionRecruitingNCT02744677Not applicable
• Hypotension Prediction Index (HPI) SMART-BP TrialTerminatedNCT05105477Not applicableResults posted
• HPI (Hypotension Prediction Index) Care TrialTerminatedNCT05083403Not applicableResults posted
• SAPIEN 3 Ultra EU PMSCompletedNCT04860752Results posted
• Pediatric Cardiac Output Monitoring Observational StudyCompletedNCT04465370Results posted
• Edwards PASCAL Transcatheter Valve Repair System RegistryCompletedNCT04443218Results posted
• Observational Registry on the HARPOON DeviceTerminatedNCT04393779Not applicableResults posted
• Treatment of Mitral Regurgitation Using a Minimally Invasive Approach With the HARPOON Device.TerminatedNCT04382612Not applicableResults posted
• 2019-06 TRISCEND StudyActive, not recruitingNCT04221490Not applicableResults posted
• PROACTIVE-HF IDE Trial Heart Failure NYHA Class IIIActive, not recruitingNCT04089059Not applicableResults posted
• Edwards CLASP TR EFSCompletedNCT03745313Not applicableResults posted
• ExCEED: CENTERA THV System in Intermediate Risk Patients Who Have Symptomatic, Severe, Calcific, Aortic StenosisActive, not recruitingNCT03517436Not applicableResults posted
• The SAPIEN 3 Ultra System in Intermediate Risk Patients With Symptomatic, Severe Aortic StenosisCompletedNCT03471065Not applicableResults posted
• Assisted Fluid Management IDE StudyCompletedNCT03469570Not applicableResults posted
• China S3: Safety and Effectiveness of Edwards Lifesciences SAPIEN 3 THV in the Chinese PopulationCompletedNCT03466918Not applicableResults posted
• China XT: Safety and Effectiveness of Edwards Lifesciences SAPIEN XT THV in the Chinese PopulationCompletedNCT03314857Not applicableResults posted
• Safety and Performance Study of the Harpoon Mitral Valve Repair SystemTerminatedNCT03285724Not applicableResults posted
• PARTNER II Trial: Placement of AoRTic TraNscathetER Valves II - Nested Registry 3/Valve-in-ValveCompletedNCT03225001Not applicableResults posted
• PARTNER II Trial: Placement of AoRTic TraNscathetER Valves II - High Risk and Nested Registry 7CompletedNCT03222141Not applicableResults posted
• PARTNER II Trial: Placement of AoRTic TraNscathetER Valves II - S3 IntermediateCompletedNCT03222128Not applicableResults posted
• PARTNER 3 Trial - Mitral Valve in ValveActive, not recruitingNCT03193801Not applicableResults posted
• The CLASP Study Edwards PASCAL TrAnScatheter Mitral Valve RePair System StudyCompletedNCT03170349Not applicableResults posted
• ALTERRA: SAPIEN 3 THV With the Alterra Adaptive PrestentActive, not recruitingNCT03130777Not applicableResults posted
• Edwards Cardioband System ACTIVE Pivotal Clinical Trial (ACTIVE)TerminatedNCT03016975Not applicableResults posted
• TRI-REPAIR: TrIcuspid Regurgitation RePAIr With CaRdioband Transcatheter SystemCompletedNCT02981953Not applicableResults posted
• EDWARDS INTUITY Elite Valve SystemCompletedNCT02907463Results posted
• A Clinical Trial of Transcatheter Aortic Valves in Dialysis Patients (Japan)Active, not recruitingNCT02903420Not applicableResults posted
• The SPACER Trial - Repair of Tricuspid Valve Regurgitation Using the Edwards TricuSPid TrAnsCatheter REpaiR SystemCompletedNCT02787408Not applicableResults posted
• Safety and Early Feasibility Study of the Harpoon Medical Device (EFS)CompletedNCT02771275Not applicableResults posted
• CE Mark Study for the Harpoon Medical DeviceCompletedNCT02768870Not applicableResults posted
• REPAIR - transcatheteR rEPair of mitrAl Insufficiency With caRdioband SystemTerminatedNCT02703311Not applicableResults posted
• EDWARDS INTUITY Valve System CADENCE StudyCompletedNCT02688153Not applicableResults posted
• PARTNER II Trial: S3iCAPCompletedNCT02687035Not applicableResults posted
• PARTNER 3 Trial: Safety and Effectiveness of the SAPIEN 3 Transcatheter Heart Valve in Low Risk Patients With Aortic StenosisActive, not recruitingNCT02675114Not applicableResults posted
• EDWARDS INTUITY Valve System CADENCE-MIS StudyCompletedNCT02672553Not applicableResults posted
• COMMENCE Pulmonary: Clinical Evaluation of Edwards Pericardial Aortic Bioprosthesis (Model 11000A) for Pulmonary Valve ReplacementCompletedNCT02656290Not applicableResults posted
• Early Feasibility Study of the Edwards FORMA Tricuspid Transcatheter Repair SystemCompletedNCT02471807Not applicableResults posted
• CE Mark Study for the Harpoon Medical Device in PolandCompletedNCT02432196Not applicableResults posted
• A Retrospective Study to Collect the Data From the Patients Who Had the Perimount Heart Valve Replacement Surgery in China During 2001 to 2007CompletedNCT02381678Results posted
• EDWARDS INTUITY Valve System FOUNDATION StudyCompletedNCT02338154Results posted
• The PARTNER II Trial: Placement of AoRTic TraNscathetER Valves - PII BCompletedNCT02184442Not applicableResults posted
• Cardioband With Transfemoral Delivery SystemCompletedNCT01841554Not applicableResults posted
• ProspeCtive, nOn-randoMized, MulticENter Clinical Evaluation of Edwards Pericardial Bioprostheses With a New Tissue Treatment Platform (COMMENCE)CompletedNCT01757665Not applicableResults posted
• Surgical Treatment of Aortic Stenosis With a Next Generation, Rapid Deployment Surgical Aortic ValveCompletedNCT01700439Not applicableResults posted
• The SOLACE-AU Clinical TrialCompletedNCT01675596Not applicableResults posted
• Clinical Trial of the Edwards Aortic Bioprosthesis, Model 11000CompletedNCT01651052Not applicableResults posted
• Surgical Treatment of Aortic Stenosis With a Next Generation Surgical Aortic ValveCompletedNCT01445171Not applicableResults posted
• PREVAIL-20J - Transfemoral Placement of 20mm Aortic Balloon Expandable Transcatheter Valve TrialCompletedNCT01419015Not applicableResults posted
• PARTNER II Trial: Placement of AoRTic TraNscathetER Valves II - XT Intermediate and High RiskCompletedNCT01314313Not applicableResults posted
• Magna Mitral - 23mmCompletedNCT01312779Not applicableResults posted
• PREVAIL-TA: Placement of Aortic Balloon Expandable Transcatheter Valves Trial (Europe)CompletedNCT01238835Not applicableResults posted
• Carpentier-Edwards PERIMOUNT Magna Ease Pericardial Bioprosthesis, Model 3300TFXCompletedNCT01171625Not applicableResults posted
• PREVAIL-J - Transfemoral & Transapical Placement of Aortic Balloon Expandable Transcatheter Valves Trial (Japan)CompletedNCT01113983Not applicableResults posted
• Magna® Mitral Pericardial Bioprostheses Post-Approval Study ProtocolCompletedNCT00853632Not applicableResults posted
• PREVAIL-TF: Transfemoral Placement of Aortic Balloon Expandable Transcatheter Valves Trial (Europe)CompletedNCT00820599Not applicableResults posted
• COMPASSION - COngenital Multicenter Trial of Pulmonic VAlve Regurgitation Studying the SAPIEN InterventIONal THVCompletedNCT00676689Not applicableResults posted
• THE PARTNER TRIAL: Placement of AoRTic TraNscathetER Valve TrialCompletedNCT00530894Not applicableResults posted
• Autus Valve Continued Access Study (CAS)Active, not recruitingNCT07466745Not applicable
• ClearSight Baby CuffCompletedNCT06834516
• J-Valve TF Early Feasibility StudyActive, not recruitingNCT06034028Not applicable
• TRISCEND JAPAN StudyActive, not recruitingNCT05760989Not applicable
• TVMR With the Innovalve System Trial - First In Human IsraelCompletedNCT05688514Not applicable
• ALT-FLOW II Trial of the Edwards APTURE Transcatheter Shunt SystemActive, not recruitingNCT05686317Not applicable
• TVMR With the Innovalve System Trial - Pilot in GeorgiaCompletedNCT05682066Not applicable
• Real-world Clinical Outcomes of the MITRIS RESILIA Mitral ValveActive, not recruitingNCT05526560
• INSPIRIS China PMCF StudyActive, not recruitingNCT05404880
• ALTERRA Post-Approval StudyActive, not recruitingNCT05378386
• TVMR With the Innovalve System Trial - TWIST-BE TWIST-PILOT-BEWithdrawnNCT05263375Not applicable
• China S3 PMS: SAPIEN 3 China Post Market Registry StudyActive, not recruitingNCT05168826
• TVMR With the Innovalve System Trial - Pilot Study in ItalyActive, not recruitingNCT05010746Not applicable
• HUDDLE: Heart Health: Understanding & Diagnosing Disease by Leveraging EchocardiogramsCompletedNCT05009589
• Autus Valve Pivotal StudyActive, not recruitingNCT05006404Not applicable
• The EU Hyprotect RegistryCompletedNCT04972266
• ExplorATory Study oF the EdWards Transcatheter Atrial Shunt System (AlT FloW Germany)WithdrawnNCT04965623Not applicable
• INSPIRIS RESILIA Aortic Valve, Valve-in-Valve Surveillance StudySuspendedNCT04902053
• COMPASSION S3 Post-Approval StudyActive, not recruitingNCT04860765
• Transcatheter Repair of Tricuspid Regurgitation With Edwards PASCAL Transcatheter Valve Repair SystemActive, not recruitingNCT04614402
• SAPIEN 3 Ultra System PMCFActive, not recruitingNCT04555967
• TRISCEND II Pivotal TrialActive, not recruitingNCT04482062Not applicable

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