REgistry on Real-Life EXperience With Left Atrial Appendage Occlusion

Completed

• Conditions: Atrial Fibrillation

• Registration Number: NCT03279406
• Lead Sponsor: University Hospital, Tours

Brief Summary

The objective of this observational non-randomized multicenter study is to compile real-world clinical characteristics and outcomes data for patients treated with LAA (left atrial appendage) closure systems in a daily clinical setting.

Detailed Description

Not available

Study Timeline

• Study Start: 2012-02-01
• Study First Submitted: 2017-09-06
• Study First Submitted QC: 2017-09-08
• Study First Posted: 2017-09-12
• Primary Completion: 2018-06-01
• Study Completion: 2018-09-01
• Status Verified: 2024-05
• Last Update Submitted: 2024-05-11
• Last Update Posted: 2024-05-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 400

Inclusion Criteria

• Patients who are eligible for a LAA occlusion device and treated with a commercially available device according to international and local guidelines and per physician discretion.

Exclusion Criteria

• None

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Major adverse cardiovascular events	From date of inclusion until the date of first documented event, whichever came first, assessed up to 60 months	Death, Ischemic stroke, Transient ischemic attack, Major hemorrhage, Thrombus on device