πŸ›οΈ Verified NIH Record β€’ Updated 2026-08-26

Repeat Ablation of Persistent Atrial Fibrillation, Including Mitral Isthmus Catheter Ablation, With the FARAPULSE Pulsed Field Ablation System (NCT06735534)

The ReMATCH Study is a Prospective, Single Arm, Open Label, Multi-center, Study Utilizing the FARAPULSE PFA System, Including the FARAWAVE and FARAPOINT PFA Catheters

🟒 Recruiting Observational / Diagnostic βš™οΈ Medical Device Protocol Sponsor: Boston Scientific Corporation

🩺 Plain-English Summary (8th-Grade Level)

The ReMATCH Study is a prospective, single arm, open label, multi-center, study utilizing the FARAPULSE PFA System, including the FARAWAVE and FARAPOINT PFA Catheters.

Who can join: Review the eligibility criteria below.

Location: Mobile Infirmary Medical Center β€” Mobile, Alabama

Age range: 18 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (41 Sites)

Showing the first 25 of 41 sites.

  • Mobile Infirmary Medical Center β€” Mobile, Alabama
  • Arrhythmia Research Group-Research Facility β€” Jonesboro, Arkansas
  • University of Southern California Hospital β€” Los Angeles, California
  • St. John's Regional Medical Center β€” Oxnard, California
  • Stanford University Medical Center β€” Stanford, California
  • South Denver Cardiology Associates, PC β€” Littleton, Colorado
  • HCA Florida Mercy Hospital β€” Miami, Florida
  • Naples Comprehensive Health β€” Naples, Florida
  • AdventHealth Orlando-Hospital β€” Orlando, Florida
  • Tampa General Hospital β€” Tampa, Florida
  • AdventHealth Tampa-Hospital β€” Tampa, Florida
  • Emory University Hospital β€” Atlanta, Georgia
  • Atrium Health Navicent The Medical Center β€” Macon, Georgia
  • Memorial Health University Medical Center β€” Savannah, Georgia
  • St. Luke's Boise Medical Center β€” Boise, Idaho
  • Advocate Christ Medical Center-Hospital β€” Oak Lawn, Illinois
  • Johns Hopkins Hospital β€” Baltimore, Maryland
  • Massachusetts General Hospital β€” Boston, Massachusetts
  • Southcoast Physicians Group β€” Fall River, Massachusetts
  • William Beaumont Hospital-Hospital β€” Royal Oak, Michigan
  • Dartmouth Hitchcock Medical Center β€” Lebanon, New Hampshire
  • Virtua Health Inc. β€” Marlton, New Jersey
  • Lovelace Medical Center β€” Albuquerque, New Mexico
  • Northwell Health β€” Manhasset, New York
  • Weill Cornell Medical University β€” New York, New York

πŸ“ž Contact the Study Coordinator

Phone: (612) 417-9538

Email: Kristin.Mathson@bsci.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—