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Study identifier: NCT04823299 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Randomized Controlled Trial- Ablation Strategy for Paroxysmal Atrial Fibrillation - Trigger and Substrate Guided Wide Area Radiofrequency Ablation Compared to Pulsed Field Ablation Pulmonary Vein Isolation

Condition: Atrial Fibrillation · Catheter Ablation · Radiofrequency Catheter Ablation  ·  Sponsor: Ottawa Heart Institute Research Corporation

PhaseNA
Planned participants556
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Atrial fibrillation (AF) is a common heart rhythm disorder affecting over a million people in North America and is associated with serious complications including stroke, heart failure, reduced quality of life, and premature death. Catheter ablation has been shown to be more effective than medications for controlling symptoms and reducing the risk of these complications; however, recurrence of AF after ablation remains a significant challenge, often due to incomplete or ineffective initial procedures. This clinical trial aims to determine whether a novel, patient-tailored ablation strategy can improve outcomes compared to the current standard-of-care approach. Participants will be randomly assigned to undergo either standard pulmonary vein isolation or a more individualized ablation procedure that identifies and targets patient-specific sources of AF. All participants will undergo the ablation procedure, receive continuous heart rhythm monitoring, and be followed over time to assess recurrence and safety outcomes.

This description comes directly from the study's public registry record.

Talk to the study team

Girish Nair, MD  ·  613-696-7272  ·  GNair@ottawaheart.ca

Sonya Jancar  ·  613-696-7000  ·  sjancar@ottawaheart.ca

Always discuss trial participation with your own doctor first.

Locations (2)

University of Ottawa Heart InstituteOttawa, Ontario, CanadaRecruiting
McGill University Health CenterMontreal, Quebec, CanadaNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT04823299