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Combined Transcatheter Aortic Valve Implantation and Percutaneous Closure of the Left Atrial Appendage — TAVI-LAAC  

Aortic Valve Disorder Clinical Trial

Official title:
Combined Transcatheter Aortic Valve Implantation and Percutaneous Closure of the Left Atrial Appendage

Clinical Trial Summary

Atrial fibrillation (AF) is a common comorbidity of patients candidates to transcatheter aortic valve implantation (TAVI). The management of chronic oral anticoagulation (OAC) for the prevention of ischemic stroke is very challenging in this population of complex and frail subjects. Since the percutaneous left atrial appendage (LAA) closure with the WATCHMAN device proved promising safety and efficacy results in randomized comparisons with OAC (current standard of care), the aim of the current study is to assess the feasibility and the early safety of performing TAVI with the Lotus System and percutaneous LAA closure with the WATCHMAN device at the same session.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02678871
Study type Interventional
Source University Hospital Inselspital, Berne
Contact
Status Terminated
Phase N/A
Start date March 8, 2017
Completion date December 31, 2022
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