RECRUITING

Concomitant LAAC/AF Ablation (Watchman FLX Pro)

Description

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).

Study Overview

Study Details

Study overview

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).

Ablation With FARAPULSE and Left Atrial Appendage Closure With Watchman for Integrated Management of Atrial Fibrillation)

Concomitant LAAC/AF Ablation (Watchman FLX Pro)

Condition
PFA Ablation and LAAC Procedures
Intervention / Treatment

-

Contacts and Locations

Delray Beach

Arrhythmia Center of South Florida, Delray Beach, Florida, United States, 33484

Jacksonville

Ascension St. Vincent's Jacksonville, Jacksonville, Florida, United States, 32204

Miami

HCA Research Institute- Mercy Hospital, Miami, Florida, United States, 37203

Indianapolis

Ascension St Vincent -Indianapolis Ascension Health, Indianapolis, Indiana, United States, 46184

Iowa City

University of Iowa Hospitals and Clinics, Iowa City, Iowa, United States, 52242

Pittsburgh

Allegheny General Hospital, Pittsburgh, Pennsylvania, United States, 15212

Austin

Texas Cardiac Arrhythmia Research Foundation, Austin, Texas, United States, 78705

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Patients who are determined by physicians to be eligible for LAAC
  • * Patients whose LAAC with Watchman FLX Pro procedures are performed concomitant following AF ablation procedure
  • * Willing and able to provide additional informed consent to the sub-study (unless waiver of consent is obtained)

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Heart Rhythm Clinical and Research Solutions, LLC,

Study Record Dates

2026-10-30