RECRUITING

Left Atrial Appendage Occlusion Registry (LAAO Registry)

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Left Atrial Appendage Occlusion Registry (LAAO Registry)

Quick Facts

Study Start:2015-12
Study Completion:2026-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT02699957

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adult patients, 18 years and older, undergoing percutaneous or epicardial left atrial appendage occlusion procedures
  1. * None

Contacts and Locations

Study Contact

Mark Fox, CHC, CHPC
CONTACT
202-375-6305
mfox@acc.org
Christina Koutras, RN, BSN
CONTACT
202-375-6387
ckoutras@acc.org

Principal Investigator

Paul Varosy, MD
STUDY_CHAIR
VA Eastern Colorado Health Care System

Study Locations (Sites)

American College of Cardiology/National Cardiovascular Data Registry (NCDR)
Washington, District of Columbia, 20037
United States

Collaborators and Investigators

Sponsor: American College of Cardiology

  • Paul Varosy, MD, STUDY_CHAIR, VA Eastern Colorado Health Care System

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2015-12
Study Completion Date2026-01

Study Record Updates

Study Start Date2015-12
Study Completion Date2026-01

Terms related to this study

Additional Relevant MeSH Terms

  • Atrial Fibrillation