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The Fourth Left Atrial Appendage Occlusion Study

Recruiting

The Fourth Left Atrial Appendage Occlusion Study (LAAOS-4)

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

1. (a) Persistent or permanent atrial fibrillation OR (b) Paroxysmal atrial fibrillation in participants with a history of ischemic stroke or systemic embolism
2. Increased risk of stroke, defined as a CHA2DS2-VASc stroke risk score of ≥ 4. \[Note: the acronym CHA2DS2-VASc stands for congestive heart failure, hypertension, age ≥75 (doubled), diabetes, stroke (doubled), vascular disease, age 65 to 74 and sex category (female).\]
3. Treatment with oral anticoagulants (Vitamin K agonist or factor Xa inhibitor) for at least 90 days prior to enrollment, AND no documented plan to discontinue treatment with oral anticoagulants for the expected duration of the trial.

Exclusion Criteria:

1. Age \< 18 years
2. Current left atrial appendage thrombus
3. Prior left atrial appendage occlusion or removal (surgical or percutaneous)
4. Prior percutaneous atrial septal defect or patent foramen ovale closure
5. Prior atrial fibrillation ablation unless evidence of recurrent qualifying atrial fibrillation present at least 30 days following ablation
6. Planned atrial fibrillation ablation within 90 days of enrollment
7. Individuals being treated with direct thrombin inhibitors
8. Women of childbearing potential unless they agree to employ effective birth control methods throughout the study
9. Anticipated life-expectancy of \< 2 years
10. Patient unable or willing to give informed consent

About the study

LAAOS-4 aims to determine if catheter-based endovascular left atrial appendage occlusion prevents ischemic stroke or systemic embolism in participants with atrial fibrillation, who remain at high risk of stroke, despite receiving ongoing treatment with oral anticoagulation.

What is being tested

Sponsor: Hamilton Health Sciences Corporation · Participants: 4,000 · Started: Nov 30, 2023

Contact the study team

Official record on ClinicalTrials.gov — NCT05963698

Locations in the U.S.

ArkansasArrhythmia Research Group, Jonesboro
CaliforniaMemorial Health Services, Fountain Valley
Cedars-Sinai Medical Center, Los Angeles
Southern California Permanente Medical Group, Pasadena
Sutter Valley Hospitals dba Sutter Institute for Medical Research, Sacramento
DelawareChristiana Care Health Services, Inc., Wilmington
FloridaThe University of South Florida, Tampa
GeorgiaEmory University, Atlanta
IdahoSt Luke's Regional Medical Center, Ltd, Boise
Kootenai Health Inc., Coeur d'Alene
IllinoisNorthwestern University, Evanston
Cardiovascular Medicine, PLLC and Unity Point Trinity Rock Island, Rock Island
IndianaCommunity Health Network Inc., Indianapolis
IowaMercyOne Iowa Heart Center, West Des Moines
KansasUniversity of Kansas Medical Center Research Institute, Inc., Kansas City
KentuckyBabtist Health Lexington, Lexington
LouisianaOchsner Clinic Foundation, New Orleans
MarylandUniversity of Maryland Baltimore, Baltimore
MassachusettsLahey Clinic Inc., Burlington
MichiganUniversity of Michigan, Ann Arbor
Henry Ford Health System, Detroit
Henry Ford Health System, Detroit
MinnesotaMayo Clinic, Rochester
MissouriSt. Louis University,, St Louis
New JerseyHackensack University Medical Center, Hackensack
New MexicoPresbyterian Healthcare Services d.b.a. Presbyterian Heart Group, Albuquerque
New YorkCornell University for and on behalf of its Joan & Sanford I. Weill Medical College and The New York Presbyterian Hospital, New York
North CarolinaMission Hospital HCA, Asheville
OhioAultman Hospital, Canton
TriHealth Inc., Cincinnati
University of Cincinnati, Cincinnati
Cleveland Clinic, Cleveland
OklahomaSaint Francis Hospital, Tulsa
PennsylvaniaThe Pennsylvania State University and The Milton S. Hershey Medical Center, Hershey
The Trustees of the University of Pennsylvania, Philadelphia
University of Pittsburgh Medical Center (UPMC) Presbyterian Heart and Vascular Institute, Pittsburgh
Rhode IslandRhode Island Hospital, Providence
TennesseeThe University of Tennessee, Memphis
TexasBaylor Research Institute, Dallas
CHRISTUS Northeast Texas Health System, Tyler
VirginiaThe Rector and Visitors of the University of Virginia, Charlottesville
WashingtonCommonSpirit Health Research Institute, Tacoma
WisconsinThe Medical College of Wisconsin, Milwaukee

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.