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

Recruiting now

Conditions studied: Atrial Fibrillation, Cardiovascular Diseases, Thromboembolism

In brief

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

Key facts

Study ID

NCT04628078

Run by

Insel Gruppe AG, University Hospital Bern

People needed

1000

Starts

2015-08-12

Expected to finish

2027-06-01

Last updated by the study team

2023-02-22

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age> 18
• Written informed consent to participate in the study
• Patients with paroxysmal, persistent, or permanent non-valvular AF and CHA2DS2-VASc Score of ≥2 that are planned for an elective LAA-closure
• Anatomic characteristics allow placement of a CE marked device, dedicated for LAAC

You may not qualify if…

• None. Considering the nature of the project, which is to prospectively collect information on all patients treated with LAAC in our center, we will only exclude patients unwilling to sign the informed consent.

Where it is running

• Bern University Hospital Inselspital — Bern, Switzerland (enrolling)

Full record on ClinicalTrials.gov

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