Abbott: Aortic Valve Stenosis trials

The registry lists 24 Aortic Valve Stenosis studies with Abbott as lead sponsor. 3 are open to participants now and 12 have results posted.

Phase 4 1No phase 23(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.

• Navitor Japan StudyRecruitingNCT07193888
• Post-Market Clinical Follow Up Study With Navitor ValveRecruitingNCT06008080
• ENVISION IDE Trial: Safety and Effectiveness of NAVITOR in Transcatheter Aortic Valve ImplantationEnrolling by invitationNCT05932615Not applicable
• Portico and Navitor India Clinical TrialCompletedNCT05171712Not applicableResults posted
• Portico Valve-in-Valve Retrospective RegistryCompletedNCT05002088Results posted
• Portico Next Generation Approval StudyActive, not recruitingNCT04011722Not applicableResults posted
• CONFIDENCE Registry to Assess Safety and Performance of Portico System to Treat Patients With Severe Aortic Stenosis.CompletedNCT03752866Not applicableResults posted
• FlexNav EU CE Mark StudyCompletedNCT03724812Not applicableResults posted
• Assessment of the St Jude Medical Portico Resheathable Aortic Valve System-Alternative AccessCompletedNCT03056573Not applicableResults posted
• Portico Re-sheathable Transcatheter Aortic Valve System US IDE TrialActive, not recruitingNCT02000115Not applicableResults posted
• 5 Year Observation of Patients With PORTICO ValvesCompletedNCT01802788Results posted
• Trifecta™ Long Term Follow-Up (LTFU) StudyCompletedNCT01593917Results posted
• Portico TAVI Implant With Transfemoral Delivery SystemCompletedNCT01493284Not applicableResults posted
• Aortic or Mitral Valve Replacement With the Biocor and Biocor SupraCompletedNCT00636987Not applicableResults posted
• Aortic Valve Replacement With Trifecta(TM)CompletedNCT00475709Not applicableResults posted
• Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System for the Treatment of Severe, Symptomatic Aortic StenosisActive, not recruitingNCT07116551Not applicable
• Early System Experience With the Abbott Balloon-expandable TAVI System: First-In-Human StudyActive, not recruitingNCT07082426Not applicable
• Assessment of the St. Jude Medical PorticoTM Re-sheathable Aortic Valve System - Alternative AccessWithdrawnNCT02088021Not applicable
• Assessment of St Jude Medical Portico Re-sheathable Transapical Aortic Valve SystemWithdrawnNCT01742598Not applicable
• Long Term Follow-up of the 23mm Portico™ Aortic Valve Implant and the St. Jude Medical Transfemoral Delivery SystemCompletedNCT01497418
• First in Human Experience of the St. Jude Medical TAVI Valve and Delivery SystemCompletedNCT01487330Not applicable
• An Observational, Prospective Evaluation of the Trifecta™ ValveCompletedNCT00727181Not applicable
• Aortic Valve Replacement With Trifecta(TM)CompletedNCT00475267Not applicable
• REST Study: Left Ventricular Regression European StudyCompletedNCT00256165Phase 4