Observational, multi-center, clinical device registry for US patients with a primary goal to observe the clinical outcomes in patients who are mapped with Volta Medical's VX1 or AF-Xplorer systems during AF ablation procedures.
Study Type
OBSERVATIONAL
Enrollment
400
Percutaneous, catheter-based ablation of atrial fibrillation
Endeavor Health
Evanston, Illinois, United States
RECRUITINGKansas City Cardiac Arrhythmia Research LLC
Overland Park, Kansas, United States
RECRUITINGNorthwell Health
New York, New York, United States
RECRUITINGPrimary Clinical Efficacy Outcome
Percentage of subjects free from clinically significant AF or atrial arrhythmia recurrences, after one or multiple ablation procedures, stratified by type of clinical workflow and ablation history.
Time frame: 12 and 24 months
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Ohio State University
Columbus, Ohio, United States
RECRUITING