LAAC-registry: Clinical Outcome After Echocardiography-guided LAA-closure

Status Recruiting

Clinical Trial Summary

The study aims at comparing, in a large cohort of consecutive clinically indicated left atrial appendage closure, clinical and imaging outcomes between different subpopulations.

Clinical Trial Description

Percutaneous left atrial appendage closure (LAAC) has established itself in clinical practice as a safe and efficient therapeutic option for atrial fibrillation patients with a relative/absolute contraindication to oral anticoagulation. The purpose of this observational study is to prospectively collect procedural and follow-up data of all patients submitted to a clinically indicate LAAC in order to assess the impact of patient characteristics, procedural technique (imaging used to guide/plan procedure, device implanted, post-procedural drug regimens, etc.) on procedural safety and efficacy. The endpoints will be assessed by means of clinical follow-up at 1-3-5 years after LAAC and imaging exams (TEE at1-3 months, CCTA at 1-13months). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04628078
Study type	Observational [Patient Registry]
Source	University Hospital Inselspital, Berne
Contact	Lorenz Räber, Prof.
Phone	31 632 09 29
Email	lorenz.raeber@insel.ch
Status	Recruiting
Phase
Start date	August 12, 2015
Completion date	June 1, 2027

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