Edwards Lifesciences: all 141 studies
Page 2 of 2. Open to participants first (22), then studies with results posted, then the rest; newest registration first within each.
- MiCLASP Post Market Clinical Follow-Up (PMCF) StudyActive, not recruitingNCT04430075
- Beating Heart Mitral Valve Repair With the HARPOON™ SystemActive, not recruitingNCT04375332Not applicable
- The ENCIRCLE TrialActive, not recruitingNCT04153292Not applicable
- SIRONA 2 Trial Heart Failure NYHA Class IIIActive, not recruitingNCT04012944Not applicable
- Exploratory Study of the Edwards APTURE Transcatheter Shunt System (ALT-FLOW Canada)Active, not recruitingNCT04000607Not applicable
- J-Valve Compassionate UseNo longer availableNCT03876964
- ClearSight System CHN StudyCompletedNCT03807622
- Hypotension Prediction Index Study (HPI Study)CompletedNCT03805217
- Transcatheter Repair of Tricuspid Regurgitation With Edwards Cardioband TR System Post Market Study (TriBAND)Active, not recruitingNCT03779490
- Edwards PASCAL CLASP IID/IIF Pivotal Clinical TrialActive, not recruitingNCT03706833Not applicable
- CENTERA PMCF: Post-Market Follow-up of the CENTERA Transcatheter Heart Valve SystemCompletedNCT03699345
- RESILIENCE Trial: Evaluation of the Durability of Aortic Bioprostheses/Valves With RESILIA Tissue in Subjects Under 65TerminatedNCT03680040
- PRODIGY Registry in NYHA Class III Heart Failure PatientsTerminatedNCT03623165
- Edwards Cardioband European Post-Market Study, MiBANDStatus unknownNCT03600688
- Clinical Study of Edwards Cardioband FIT Valve Repair SystemActive, not recruitingNCT03382457Not applicable
- SIRONA Trial Heart Failure NYHA Class IIICompletedNCT03375710Not applicable
- CLEAR Sepsis Clinical StudyStatus unknownNCT03231956
- SAPIEN M3 EFS: Early Feasibility Study of the Edwards SAPIEN M3 System for the Treatment of Mitral RegurgitationCompletedNCT03230747Not applicable
- EARLY TAVR: Evaluation of TAVR Compared to Surveillance for Patients With Asymptomatic Severe Aortic StenosisActive, not recruitingNCT03042104Not applicable
- Safety & Efficacy of the J-Valve Ausper System in Patients With Severe Aortic Stenosis and/or Aortic RegurgitationCompletedNCT03025971Not applicable
- COMPASSION XT PAS - Post-approval Study of the SAPIEN XT THV in Patients With Pulmonary Valve DysfunctionCompletedNCT02987387
- CardiAQ-Edwards™ Transcatheter Mitral Valve Replacement (TMVR) StudyWithdrawnNCT02722551Phase 1/2
- Edwards EVOQUE Eos MISCEND StudyActive, not recruitingNCT02718001Not applicable
- SOURCE 3: Observational Study to Evaluate Safety and Performance of SAPIEN 3 THV System in Real Life PracticeCompletedNCT02698956
- Clinical Study to Evaluate the Performance of Magna Ease Heart Valve in Chinese PatientsTerminatedNCT02523066
- Early Feasibility Study of the CardiAQ™ TMVI System (Transfemoral and Transapical DS)WithdrawnNCT02515539Not applicable
- A Clinical Study of the CardiAQ™ TMVI System (Transapical DS)TerminatedNCT02478008Not applicable
- CENTERA-2: Safety and Performance Study of the Edwards CENTERA-EU Self-Expanding Transcatheter Heart ValveCompletedNCT02458560Not applicable
- Clinical Study to Evaluate the Performance of Perimount Heart Valve in Chinese PatientsCompletedNCT02400489
- GlucoClear ICU StudyWithdrawnNCT02238041
- GlucoClearTM System ICU StudyCompletedNCT02094859
- Safety and Performance Study of the Edwards SAPIEN 3 Transcatheter Heart Valve/ The SAPIEN 3 StudyCompletedNCT01808287Not applicable
- Safety and Performance Study of the Edwards CENTERA Self-Expanding Transcatheter Heart ValveCompletedNCT01808274Not applicable
- MITRAFIT- Cardinal Adjustable Mitral Repair Follow-up International Postmarketing Surveillance (PMS)CompletedNCT01617720
- V-Chordal Adjustable System for Chordal Replacement in Mitral Valve Insufficiency Due to Leaflet ProlapseTerminatedNCT01415947Phase 2
- Clinical Evaluation of a New Transpulmonary Thermodilution Method to Assess Thermodilution Cardiac Output, Global End Diastolic Volume and Extravascular Lung WaterCompletedNCT01405040
- Pulmonic Valve REplacement Multi-discIpline EMEA RegistryCompletedNCT01356108
- SOURCE XT REGISTRYCompletedNCT01238497
- CARDINAL Adjustable Annuloplasty Ring System For Treatment of Mitral RegurgitationCompletedNCT01137734Not applicable
- Clinical Study of the Intravenous Blood Glucose System in Hospitalized Adult Elective or Non-Emergent Surgery and Medical/Surgical Intensive Care Unit PatientsCompletedNCT00906490
- Using Minimally Invasive Cardiac Output Data vs. Standard Care for Patients Emergently Admitted to the Intensive Care Unit Who Are Hemodynamically UnstableCompletedNCT00354211