Aortic Valve Stenosis: all 1,006 studies

Page 4 of 11. Open to participants first (284), then studies with results posted, then the rest; newest registration first within each.

• FlexNav EU CE Mark StudyCompletedNCT03724812Not applicableResults posted
• REPRISE IV: LOTUS Edge Valve System in Intermediate Surgical Risk SubjectsTerminatedNCT03618095Not applicableResults posted
• ExCEED: CENTERA THV System in Intermediate Risk Patients Who Have Symptomatic, Severe, Calcific, Aortic StenosisActive, not recruitingNCT03517436Not applicableResults posted
• Targeting Pulsatile Load to Increase Exercise Capacity and Quality of Life After Aortic Valve Replacement for Severe Aortic Stenosis (PULSE AS)CompletedNCT03483051Phase 2Results posted
• The SAPIEN 3 Ultra System in Intermediate Risk Patients With Symptomatic, Severe Aortic StenosisCompletedNCT03471065Not applicableResults posted
• China S3: Safety and Effectiveness of Edwards Lifesciences SAPIEN 3 THV in the Chinese PopulationCompletedNCT03466918Not applicableResults posted
• A Prospective Study of Fractional Flow Reserve Assessment of Intermediate Coronary Stenoses in Severe Aortic StenosisTerminatedNCT03442400Not applicableResults posted
• Transmural Systems Transcaval Closure Device for Transcaval Access Ports During Transcatheter Aortic Valve ReplacementTerminatedNCT03432494Not applicableResults posted
• China XT: Safety and Effectiveness of Edwards Lifesciences SAPIEN XT THV in the Chinese PopulationCompletedNCT03314857Not 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
• WATCH-TAVR, WATCHMAN for Patients With Atrial Fibrillation Undergoing Transcatheter Aortic Valve ReplacementCompletedNCT03173534Not applicableResults posted
• Assessment of the St Jude Medical Portico Resheathable Aortic Valve System-Alternative AccessCompletedNCT03056573Not applicableResults posted
• EDWARDS INTUITY Elite Valve SystemCompletedNCT02907463Results posted
• A Clinical Trial of Transcatheter Aortic Valves in Dialysis Patients (Japan)Active, not recruitingNCT02903420Not applicableResults posted
• Comparison of a Rivaroxaban-based Strategy With an Antiplatelet-based Strategy Following Successful TAVR for the Prevention of Leaflet Thickening and Reduced Leaflet Motion as Evaluated by Four-dimensional, Volume-rendered Computed Tomography (4DCT)CompletedNCT02833948Phase 3Results posted
• Home-Based Exercise Program For Recovery After Transcatheter Aortic Valve ReplacementCompletedNCT02805309Not applicableResults posted
• Association of Type of Anesthetic and Outcomes in Transfemoral Aortic Valve ReplacementCompletedNCT02786264Results posted
• Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)CompletedNCT02746809Not applicableResults posted
• The Medtronic TAVR 2.0 US Clinical StudyCompletedNCT02738853Not applicableResults posted
• JENAVALVE AS EFS TRIAL: Pericardial TAVR Aortic Stenosis StudyStatus unknownNCT02732691Not applicableResults posted
• Medtronic Evolut Transcatheter Aortic Valve Replacement in Low Risk PatientsActive, not recruitingNCT02701283Not applicableResults posted
• EDWARDS INTUITY Valve System CADENCE StudyCompletedNCT02688153Not applicableResults posted
• PARTNER II Trial: S3iCAPCompletedNCT02687035Not applicableResults posted
• PERIGON Japan TrialCompletedNCT02686814Not 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
• Perceval Sutureless Implant Versus Standard-Aortic Valve ReplacementTerminatedNCT02673697Not applicableResults posted
• EDWARDS INTUITY Valve System CADENCE-MIS StudyCompletedNCT02672553Not applicableResults posted
• Self-Centering Guide Catheter Feasibility StudyCompletedNCT02639494Not applicableResults posted
• The REFLECT Trial: Cerebral Protection to Reduce Cerebral Embolic Lesions After Transcatheter Aortic Valve ImplantationCompletedNCT02536196Not applicableResults posted
• Inflammation and Thrombosis in Patients With Severe Aortic Stenosis After Transcatheter Aortic Valve Replacement (TAVR)CompletedNCT02486367Phase 4Results posted
• A Study Evaluating the Effects of Ataciguat (HMR1766) on Aortic Valve CalcificationCompletedNCT02481258Phase 2Results posted
• Neuroprotection in Patients Undergoing Aortic Valve ReplacementCompletedNCT02389894Not applicableResults posted
• EDWARDS INTUITY Valve System FOUNDATION StudyCompletedNCT02338154Results posted
• Cerebral Protection in Transcatheter Aortic Valve ReplacementCompletedNCT02214277Not applicableResults posted
• Medtronic CoreValve Evolut R U.S. Clinical StudyCompletedNCT02207569Not applicableResults posted
• Safety and Efficacy Study of Lotus Valve for Transcatheter Aortic Valve ReplacementTerminatedNCT02202434Not applicableResults posted
• The PARTNER II Trial: Placement of AoRTic TraNscathetER Valves - PII BCompletedNCT02184442Not applicableResults posted
• PERIGON Pivotal TrialActive, not recruitingNCT02088554Not applicableResults posted
• RESPOND Post Market StudyCompletedNCT02031302Results posted
• Portico Re-sheathable Transcatheter Aortic Valve System US IDE TrialActive, not recruitingNCT02000115Not applicableResults posted
• Progel Vascular SealantCompletedNCT01959503Not applicableResults posted
• The Medtronic CoreValve™ Evolut R™ CE Mark Clinical StudyCompletedNCT01876420Not applicableResults posted
• 5 Year Observation of Patients With PORTICO ValvesCompletedNCT01802788Results posted
• Engager Direct Aortic Clinical StudyCompletedNCT01789567Not 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
• ADVANCE Direct Aortic StudyCompletedNCT01676727Results posted
• The SOLACE-AU Clinical TrialCompletedNCT01675596Not applicableResults posted
• Open-label, Randomized Trial in Participants Undergoing TAVR to Determine Safety & Efficacy of Bivalirudin vs UFHCompletedNCT01651780Phase 3Results posted
• Clinical Trial of the Edwards Aortic Bioprosthesis, Model 11000CompletedNCT01651052Not applicableResults posted
• Hemodynamic Comparison of Tissue Aortic ValvesCompletedNCT01635244Not applicableResults posted
• Clinical Evaluation of MDT-2111 in Subjects With Small Aortic Annuli and Symptomatic Severe Aortic StenosisCompletedNCT01634269Not applicableResults posted
• CoreValve Advance-II Study: Prospective International Post-market StudyCompletedNCT01624870Results posted
• Correlation of Auscultatory Severity of Aortic Stenosis With Trans Thoracic EchocardiographyCompletedNCT01605669Results posted
• Trifecta™ Long Term Follow-Up (LTFU) StudyCompletedNCT01593917Results posted
• Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment of Severe, Symptomatic Aortic Stenosis in Intermediate Risk Subjects Who Need Aortic Valve Replacement (SURTAVI).Active, not recruitingNCT01586910Not applicableResults posted
• Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve ReplacementCompletedNCT01531374Not applicableResults posted
• Portico TAVI Implant With Transfemoral Delivery SystemCompletedNCT01493284Not applicableResults posted
• DEFLECT I: Keystone Heart Embolic Deflection TrialCompletedNCT01448421Not applicableResults posted
• Surgical Treatment of Aortic Stenosis With a Next Generation Surgical Aortic ValveCompletedNCT01445171Not applicableResults posted
• Clinical Evaluation of MDT-2111 in Subjects With Symptomatic Severe Aortic StenosisCompletedNCT01437098Not applicableResults posted
• PREVAIL-20J - Transfemoral Placement of 20mm Aortic Balloon Expandable Transcatheter Valve TrialCompletedNCT01419015Not applicableResults posted
• REpositionable Percutaneous Replacement of Stenotic Aortic Valve Through Implantation of Lotus™ Valve SystEmCompletedNCT01383720Not applicableResults posted
• Microembolic Signals and Cerebrospinal Fluid Markers of Neuronal Damage After Surgical Aortic Valve ReplacementCompletedNCT01319799Results posted
• PARTNER II Trial: Placement of AoRTic TraNscathetER Valves II - XT Intermediate and High RiskCompletedNCT01314313Not applicableResults posted
• Aortic Stenosis and PhosphodiEsterase Type 5 iNhibition (ASPEN): A Pilot StudyTerminatedNCT01275339Phase 4Results posted
• Aortic Stenosis and PhosphodiEsterase iNhibition With Aortic Valve Replacement (ASPEN-AVR): A Pilot StudyTerminatedNCT01272388Phase 4Results posted
• Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in High Risk and Very High Risk Subjects Who Need Aortic Valve ReplacementCompletedNCT01240902Not applicableResults posted
• PREVAIL-TA: Placement of Aortic Balloon Expandable Transcatheter Valves Trial (Europe)CompletedNCT01238835Not applicableResults posted
• The Effect of the Hyperinsulinemic Normoglycemic Clamp on Myocardial Function and Utilization of GlucoseCompletedNCT01187329Not 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
• CryoValve SG Pulmonary Human Heart Valve Post Clearance StudyCompletedNCT01092442Results posted
• CoreValve Advance International Post Market StudyCompletedNCT01074658Results posted
• Acute Hemodynamic Effects of Sildenafil in Patients With Severe Aortic StenosisCompletedNCT01060020Phase 4Results posted
• Clinical Evaluation of Percutaneous Implantation of the Medtronic CoreValve Aortic Valve Prosthesis (18Fr-Study)CompletedNCT01051518Not applicableResults posted
• Medtronic CoreValve REDO StudyCompletedNCT01051310Not applicableResults posted
• CoreValve® System Australia/New Zealand Clinical StudyCompletedNCT01015612Not applicableResults posted
• PREVAIL-TF: Transfemoral Placement of Aortic Balloon Expandable Transcatheter Valves Trial (Europe)CompletedNCT00820599Not applicableResults posted
• Aortic or Mitral Valve Replacement With the Biocor and Biocor SupraCompletedNCT00636987Not applicableResults posted
• The Effect of Lipitor on Aortic StenosisTerminatedNCT00590135Phase 4Results posted
• Radiation Following Percutaneous Balloon Aortic Valvuloplasty to Prevent RestenosisTerminatedNCT00538759Phase 2/3Results posted
• THE PARTNER TRIAL: Placement of AoRTic TraNscathetER Valve TrialCompletedNCT00530894Not applicableResults posted
• Aortic Valve Replacement With Trifecta(TM)CompletedNCT00475709Not applicableResults posted
• An Investigational Drug on Clinical Outcomes in Patients With Aortic Stenosis (Narrowing of the Major Blood Vessel of the Heart)(MK-0653A-043 AM4)(COMPLETED)CompletedNCT00092677Phase 3Results posted
• Quality of Life After Transcatheter Aortic Valve ImplantationActive, not recruitingNCT07798713
• TAVI in LOW RISK in the REAL WORLDCompletedNCT07605780
• Post-Dilatation in Balloon-Expandable TAVI ProsthesesActive, not recruitingNCT07477002Not applicable
• Electrophysiological Outcomes After Transcatheter Aortic Valve ReplacementActive, not recruitingNCT07390513
• Echocardiography Findings in Patients With Myocardial Fibrosis and Severe Aortic StenosisCompletedNCT07331116
• Alwide Plus China Post-market Clinical InvestigationCompletedNCT07304427
• Pre- and Post-TAVI Patient Assessment: Advancing Outcome Precision in Aortic Valve TherapyCompletedNCT07179302
• Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System for the Treatment of Severe, Symptomatic Aortic StenosisActive, not recruitingNCT07116551Not applicable
• Perceval Aortic Bioprostheses : Durability Study.CompletedNCT07116265
• Atrial Amyloid May Influence Outcomes in Patients Undergoing Surgical Aortic Valve ReplacementCompletedNCT07105501
• Early System Experience With the Abbott Balloon-expandable TAVI System: First-In-Human StudyActive, not recruitingNCT07082426Not applicable
• Study on Heart Block Risks Using Outcome-Based ModelingCompletedNCT07065123
• ACURATE Enhance Post Market StudyWithdrawnNCT06959862

← Aortic Valve Stenosis overview