Left Atrial Appendage Occlusion Registry (LAAO Registry)

Part of paid clinical trials in Washington D.C., District of Columbia.

Sponsor
American College of Cardiology
Study ID
NCT02699957
Status
Recruiting
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Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Left Atrial Appendage Occlusion — PROCEDURE
    Patients undergoing percutaneous/epicardial intervention for left atrial appendage occlusion.

Study Details

The Left Atrial Appendage Occlusion Registry (LAAO Registry™) is designed to assess the prevalence, demographics, management, and outcomes of patients undergoing percutaneous and epicardial based left atrial appendage occlusion procedures to reduce the risk of stroke. Patient-level data will be submitted by participating hospitals on a quarterly basis to the American College of Cardiology Foundation's National Cardiovascular Data Registry (NCDR). The primary aims of the LAAO Registry are to optimize the outcomes and management of patients through the implementation of evidence-based guideline recommendations in clinical practice, facilitate efforts to improve the quality and safety for patients undergoing percutaneous and epicardial based left atrial appendage procedures, investigate novel quality improvement methods and provide risk-adjusted assessment of patients for comparison with nationwide NCDR data. The secondary purpose of the LAAO Registry is to serve as a rich source of clinical data to support assessments of short- and long-term safety, comparative and cost effectiveness research, and as a scalable data infrastructure for post market studies.

Key Dates

Start date
Dec 31, 2015
Status verified
Jun 2026
Primary completion
Jan 31, 2029
Completion
Jan 31, 2029

Study Design

Enrollment
3,000 participants (estimated)

Arms

  • Arm: Atrial Fibrillation
    Those patients with the condition of atrial fibrillation.

Primary Outcome Measure

Proportion of patients with a major complication [ Time Frame: Assessed in hospital for any occurence from the start of procedure date and time until discharge date and time, assessed up to 24 months. Reported quarterly. ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
American College of Cardiology/National Cardiovascular Data Registry (NCDR)Washington D.C.District of Columbia20037
NCDR Product Support
[email protected]
1-800-257-4737

Find similar trials in Washington D.C., DC

By condition
Atrial fibrillation
By specialty
CardiologyHeart disease
By research site
American College of Cardiology/National Cardiovascular Data Registry (NCDR)· Washington D.C., DC

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