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Randomized Ablation-based AF Rhythm-control Versus Rate-control in Patients With HF and High-burden AF Extend

Atrial Fibrillation | Heart Failure

This is an extended follow up study of the original RAFT-AF Study. The RAFT-AF study was a multi-centre randomized controlled trial with a prospective randomized open blinded endpoint trial (PROBE) design. Patients were randomized to either catheter ablation-based rhythm control of AF as compared to rate control of AF

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Participation Requirements

  • Sex:

    ALL

  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria:

All patients previously enrolled and randomized in the RAFT-AF Study that are eligible to enroll

Exclusion Criteria:

* Did not participate in the original RAFT-AF Study

Study Location

Victoria Cardiac Arrhythmia Trials
Victoria Cardiac Arrhythmia Trials
Victoria, British Columbia
Canada

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St. Mary's General Hospital
St. Mary's General Hospital
Kitchener, Ontario
Canada

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Montreal Heart Institute
Montreal Heart Institute
Montréal, Quebec
Canada

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Libin Cardiovascular Institute
Libin Cardiovascular Institute
Calgary, Alberta
Canada

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Kingston General Hospital
Kingston General Hospital
Kingston, Ontario
Canada

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Primary Contact

Damian Redfearn, M.D.

[email protected]
613-549-6666
McGill University Health Centre
McGill University Health Centre
Montréal, Quebec
Canada

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Queen Elizabeth II Health Science
Queen Elizabeth II Health Science
Halifax, Nova Scotia
Canada

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London Health Science Centre
London Health Science Centre
London, Ontario
Canada

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CHUS Le Centre hospitalier universitaire de Sherbrooke
CHUS Le Centre hospitalier universitaire de Sherbrooke
Sherbrooke, Quebec
Canada

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Primary Contact

Jean-Francois Roux, M.D.

[email protected]
819-346-1110
Hamilton Health Sciences Centre
Hamilton Health Sciences Centre
Hamilton, Ontario
Canada

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University of Ottawa Heart Institute
University of Ottawa Heart Institute
Ottawa, Ontario
Canada

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Study Sponsored By
London Health Sciences Centre Research Institute and Lawson Research Institute of St. Joseph's
Participants Required
More Information
Study ID: NCT05118893