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The Fourth Left Atrial Appendage Occlusion Study

Atrial Fibrillation | Stroke, Ischemic | Systemic Embolism

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.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation 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

Study Location

University of Calgary
University of Calgary
Calgary, Alberta
Canada

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Cambridge Cardiac Care Inc.
Cambridge Cardiac Care Inc.
Cambridge, Ontario
Canada

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Southlake Regional Health Centre
Southlake Regional Health Centre
Newmarket, Ontario
Canada

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Sunnybrook Health Sciences Center
Sunnybrook Health Sciences Center
Toronto, Ontario
Canada

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Institut universitaire de cardiologie et de pneumologie de Québec-Université Laval
Institut universitaire de cardiologie et de pneumologie de Québec-Université Laval
Québec, Quebec
Canada

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Circulate Cardiac & Vascular Centre (CCVC)
Circulate Cardiac & Vascular Centre (CCVC)
Burlington, Ontario
Canada

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Lawson Health Research Institute
Lawson Health Research Institute
London, Ontario
Canada

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Niagara Health System - Niagara Falls
Niagara Health System - Niagara Falls
St. Catharines, Ontario
Canada

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Centre hospitalier de l'Université de Montréal
Centre hospitalier de l'Université de Montréal
Montréal, Quebec
Canada

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Vancouver Coastal Health Authority
Vancouver Coastal Health Authority
Vancouver, British Columbia
Canada

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Hamilton Health Sciences Corp
Hamilton Health Sciences Corp
Hamilton, Ontario
Canada

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Ottawa Heart Institute Research Corp
Ottawa Heart Institute Research Corp
Ottawa, Ontario
Canada

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Lawrence Park Cardiology
Lawrence Park Cardiology
Toronto, Ontario
Canada

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Centre intégré universitaire de santé et de services sociaux de l'Estrie - Centre hospitalier universitaire de Sherbrooke (CIUSSS de l'Estrie - CHUS)
Centre intégré universitaire de santé et de services sociaux de l'Estrie - Centre hospitalier universitaire de Sherbrooke (CIUSSS de l'Estrie - CHUS)
Sherbrooke, Quebec
Canada

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St. Boniface Hospital Inc.
St. Boniface Hospital Inc.
Winnipeg, Manitoba
Canada

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Waterloo Wellington Cardiovascular Research Institute (WWCRI)
Waterloo Wellington Cardiovascular Research Institute (WWCRI)
Kitchener, Ontario
Canada

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Niagara Health Systems - St. Catharines
Niagara Health Systems - St. Catharines
St Catharines, Ontario
Canada

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Institut de Cardiologie de Montreal (ICM)
Institut de Cardiologie de Montreal (ICM)
Montréal, Quebec
Canada

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Study Sponsored By
Hamilton Health Sciences Corporation
Participants Required
More Information
Study ID: NCT05963698