Concomitant LAAC/AF Ablation (Watchman FLX Pro)

Running, not enrolling

Conditions studied: PFA Ablation and LAAC Procedures

In brief

This sub-study is a prospective/retrospective, non-randomized, observational, comparative cohorts study, embedded in and expanding on the infrastructure of a real-world AF ablation registry DISRUPT-AF (NCT06335082).

Key facts

Study ID

NCT07041125

Run by

Heart Rhythm Clinical and Research Solutions, LLC

People needed

120

Starts

2025-06-01

Expected to finish

2026-10-30

Last updated by the study team

2026-07-15

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

• Arrhythmia Institute at Grandview — Birmingham, Alabama, United States
• Arrhythmia Center of South Florida — Delray Beach, Florida, United States
• Ascension St. Vincent's Jacksonville — Jacksonville, Florida, United States
• HCA Research Institute- Mercy Hospital — Miami, Florida, United States
• Ascension St Vincent -Indianapolis Ascension Health — Indianapolis, Indiana, United States
• University of Iowa Hospitals and Clinics — Iowa City, Iowa, United States
• Norton Heart & Vascular Institute — Louisville, Kentucky, United States
• Allegheny General Hospital — Pittsburgh, Pennsylvania, United States
• Texas Cardiac Arrhythmia Research Foundation — Austin, Texas, United States
• St, Mark's Hospital — Salt Lake City, Utah, United States
• Chippenham Hospital) — Richmond, Virginia, United States

Full record on ClinicalTrials.gov

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