Clinical Research Directory

Inclusion Criteria: * Patients who, in the opinion of the investigator, are candidates for ablation to treat atrial fibrillation. * Plans to undergo an ablation procedure using the TactiFlex Ablation Catheter™, Sensor Enabled™ (TactiFlex SE) manufactured by Abbott. * De Novo or redo AF catheter ablation procedures. * Able and willing to participate in baseline and all follow up evaluations. * 18 years of age or older. Exclusion Criteria: * Enrolled in any other cardiac device clinical trial, investigational drug trial, or any other trial that may confound the results of the ablation procedure. * In the opinion of the investigator, any known contraindication to an ablation procedure or to any device or drug required for use during an ablation procedure as assessed by the investigator.