Registry for patients undergoing left atrial appendage occlusion procedures

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The Left Atrial Appendage Occlusion Registry (LAAO Registry) collects data on patients who undergo procedures to occlude the left atrial appendage, aimed at reducing stroke risk in individuals with atrial fibrillation. Participating hospitals submit patient-level data quarterly to the American College of Cardiology Foundation's National Cardiovascular Data Registry. The registry aims to optimize patient outcomes through evidence-based guidelines, improve quality and safety in clinical practice, and facilitate risk-adjusted assessments for comparison with nationwide data. It serves as a valuable resource for quality improvement and clinical research.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adult patients, 18 years and older, undergoing percutaneous or epicardial left atrial appendage occlusion procedures

Exclusion Criteria:

* None

Where it's running

• American College of Cardiology/National Cardiovascular Data Registry (NCDR)
  Washington D.C., District of Columbia, United States Recruiting

Study contacts

• Study coordinator: Mark Fox, CHC, CHPC
• Email: mfox@acc.org
• Phone: 202-375-6305

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.