πŸ›οΈ Verified NIH Record β€’ Updated 2026-07-30

A Study Assessing Long-Term Safety and Effectiveness in Treatment Management of Atrial Fibrillation With VARIPULSE Catheter System (NCT07227532)

BWI202405: Assessment of Long-Term Safety and Effectiveness in Treatment Management of Atrial Fibrillation With the VARIPULSEβ„’ Catheter System

🟒 Recruiting Observational / Diagnostic βš™οΈ Medical Device Protocol Sponsor: Biosense Webster, Inc.

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

The purpose of this study is to evaluate the long-term safety and effectiveness of the FDA approved VARIPULSE catheter system for pulmonary vein isolation (PVI) in the treatment of participants with symptomatic paroxysmal atrial fibrillation (PAF).

Who can join: Review the eligibility criteria below.

Location: Phoenix Cardiovascular Research Group β€” Phoenix, Arizona

Age range: 22 Years

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 (23 Sites)

  • Phoenix Cardiovascular Research Group β€” Phoenix, Arizona
  • Tucson Medical Center Pima Heart and Vascular β€” Tucson, Arizona
  • OC Memorial β€” Fountain Valley, California
  • San Diego Cardiac Center β€” San Diego, California
  • Stanford Hospital and Clinics β€” Stanford, California
  • Community Memorial Hospital β€” Ventura, California
  • Aurora Denver Cardiology Associates β€” Aurora, Colorado
  • Colorado Heart and Vascular PC β€” Golden, Colorado
  • HCA Florida Mercy Hospital β€” Miami, Florida
  • Orlando Health Heart and Vascular Institute β€” Orlando, Florida
  • Deaconess Gateway Hospital β€” Newburgh, Indiana
  • The Kansas City Heart Rhythm Institute β€” Overland Park, Kansas
  • Norton Heart and Vascular Institute β€” Louisville, Kentucky
  • Trinity Health β€” Ypsilanti, Michigan
  • Mayo Clinic Rochester β€” Rochester, Minnesota
  • Albert Einstein College Of Medicine - Montefiore Medical Center β€” The Bronx, New York
  • The Christ Hospital β€” Cincinnati, Ohio
  • Springfield Medical Center β€” Springfield, Ohio
  • Texas Cardiac Arrhythmia Research Foundation β€” Austin, Texas
  • Baylor Scott and White Research Institute β€” Fort Worth, Texas
  • Baylor Scott & White Research Institute at The Heart Hospital Baylor Plano β€” Plano, Texas
  • Winchester Medical Center β€” Winchester, Virginia
  • Mercy Hospital β€” Janesville, Wisconsin

πŸ“ž Contact the Study Coordinator

Phone: (949) 230-3701

Email: EPurcel1@its.jnj.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†—