Medtronic: Aortic Valve Stenosis trials

The registry lists 32 Aortic Valve Stenosis studies with Medtronic as lead sponsor. 1 are open to participants now and 21 have results posted.

No phase 32(a study in two phases counts in both)

Studies

Open to participants first, then studies with results posted, then the rest; newest registration first within each.

• REdo tranScatheter Aortic Valve Replacement for Transcatheter aOrtic Valve failuRERecruitingNCT06777368
• SMall Annuli Randomized To Evolut™ or SAPIEN™ TrialActive, not recruitingNCT04722250Not applicableResults posted
• Medtronic Evolut™ EXPAND TAVR I Feasibility StudyTerminatedNCT04639258Not applicableResults 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
• Medtronic Evolut Transcatheter Aortic Valve Replacement in Low Risk PatientsActive, not recruitingNCT02701283Not applicableResults posted
• PERIGON Japan TrialCompletedNCT02686814Not applicableResults posted
• Medtronic CoreValve Evolut R U.S. Clinical StudyCompletedNCT02207569Not applicableResults posted
• PERIGON Pivotal TrialActive, not recruitingNCT02088554Not applicableResults posted
• The Medtronic CoreValve™ Evolut R™ CE Mark Clinical StudyCompletedNCT01876420Not applicableResults posted
• Engager Direct Aortic Clinical StudyCompletedNCT01789567Not applicableResults posted
• ADVANCE Direct Aortic StudyCompletedNCT01676727Results 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
• 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
• Clinical Evaluation of MDT-2111 in Subjects With Symptomatic Severe Aortic StenosisCompletedNCT01437098Not applicableResults 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
• CoreValve Advance International Post Market StudyCompletedNCT01074658Results 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
• FORWARD PRO Study Interventional Post-market Study With the Evolut™ PRO SystemCompletedNCT03417011
• The Medtronic Transcatheter Aortic Valve Implant System (CoreValve System Family) Post Marketing Surveillance (PMS) (CoreValve India PMS)TerminatedNCT02759237
• CoreValve™ Evolut R™ FORWARD StudyCompletedNCT02592369
• CoreValve VIVA Study Evaluation of the Clinical Outcomes of CoreValve in Degenerative Surgical Aortic Bioprosthesis.CompletedNCT02209298
• Engager Align Post-market Clinical StudyCompletedNCT02149654
• Enable® Aortic Sutureless Bioprosthesis EvaluationCompletedNCT01720342
• Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptomatic Severe Aortic Stenosis With Significant Comorbidities in Extreme Risk Subjects Who Need Aortic Valve ReplacementCompletedNCT01675440
• Enable I Long-term Follow-up StudyTerminatedNCT01636648
• Post-Approval Study for the MOSAIC® BioprosthesesCompletedNCT01574625
• Transapical Implantation of the Medtronic Engager Transcatheter Aortic Valve Implantation System - The Engager European Pivotal TrialCompletedNCT01348438Not applicable