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Study identifier: NCT06335082 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Enrolling By Invitation

A Registry Based Collaborative to Measure Efficiency, Effectiveness, and Safety of Farapulse PFA Technology for AF

Condition: Atrial Fibrillation  ·  Sponsor: Heart Rhythm Clinical and Research Solutions, LLC

PhaseN/A
Planned participants10000
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The DISRUPT-AF Registry is an observational, prospective, multi-center, non-randomized, real-world registry designed to obtain clinical experience with the Farapulse Pulsed Field Ablation System for the treatment of atrial fibrillation (AF).

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

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (35)

Arrhythmia Institute at GrandviewBirmingham, Alabama, United States
Arrhythmia Research GroupJonesboro, Arkansas, United States
Sutter Health - California Pacific Medical CenterSan Francisco, California, United States
Community Memorial Health SystemsVentura, California, United States
South Denver Cardiology AssociatesLittleton, Colorado, United States
The Arrythmia Center of South FloridaDelray Beach, Florida, United States
Ascension St. Vincent'sJacksonville, Florida, United States
HCA Florida Mercy HospitalMiami, Florida, United States
Sarasota Memorial HospitalSarasota, Florida, United States
St. Luke's Medical CenterBoise, Idaho, United States
Endeavor Health (Northshore)Glenview, Illinois, United States
Ascension St Vincent -Indianapolis Ascension HealthIndianapolis, Indiana, United States

+ 23 more locations — full list on the registry record.

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