IRB Study Number 19-114
Status Recruiting
Location Cleveland Clinic Main Campus
Institute Heart and Vascular Institute
Description
The purpose of this study is to provide additional information about the safety and effectiveness of the VISITAG SURPOINT™ Module with External Processing Unit (EPU) when used with a THERMOCOOL SMARTTOUCH® SF (STSF) and THERMOCOOL SMARTTOUCH® (ST) catheter.
Inclusion Criteria
- Patient has symptomatic paroxysmal atrial fibrillation, and had at least one AF episode documented within 1 year prior to enrollment
- Failed at least one antiarrhythmic drug
Exclusion Criteria
- Patient has previously had surgical or catheter ablation for atrial fibrillation
- Unstable angina
