A Study Assessing Long-Term Safety and Effectiveness in Treatment Management of Atrial Fibrillation With VARIPULSE Catheter System
Listed focus: Atrial Fibrillation
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).
- Basic eligibility summary
- Ages 22 Years
- Locations
- Phoenix, Arizona · Tucson, Arizona · Fountain Valley, California · +20 more
Eligibility summary from the record
* Symptomatic paroxysmal Atrial Fibrillation (AF) who, in the opinion of the investigator, are candidates for catheter ablation for AF * Refractory (that is, ineffective, not tolerated, or not desired) or contraindicated to at least one Class I/III antiarrhythmic drugs (AAD) * Willing and capable of providing consent…
Summarized from the sponsor's posted criteria. The research site makes the final eligibility decision.
Sponsor / responsible party: Biosense Webster, Inc.
Source: ClinicalTrials.gov · Record updated July 30, 2026 · Last checked by BrightStudy August 1, 2026
Compensation is not stated for this listing. BrightStudy does not add compensation information unless it is independently verified with the study partner.
View the full record on ClinicalTrials.gov