Re-Ablation Using a Tailored Approach Targeting EGM-Dispersion

Prior treatment

• Previous ablation procedure-related complication (e.g. fistula, perforation, etc.)
• Long-standing persistent AF recurrence prior to study redo procedure
• Previous AF ablation using VX1 software
• LA thrombus on Transesophageal Echocardiography (TEE)\* or CT Scan prior to procedure
• Previous AV valve surgery
• Enrollment in an investigational study evaluating another device, biologic, or drug

Other illness

• Any cardiac surgery except catheter ablation within the past 2 months (60 days) (includes PCI)
• Myocardial infarction within the past 2 months (60 days)
• History of blood clotting or bleeding abnormalities
• Rheumatic Heart Disease
• Cardiac Sarcoidosis
• Awaiting cardiac transplantation or other cardiac surgery within the next 12 months (365 days)
• Unstable angina within the past month
• Acute illness or active systemic infection or sepsis
• AF secondary to electrolyte imbalance, thyroid disease, or reversible or non-cardiac cause
• Significant severe pulmonary disease (e.g. patients with restrictive pulmonary disease, constrictive or chronic obstructive pulmonary disease in GOLD stage IV) or any other disease or malfunction of the lungs or respiratory system that produces chronic symptoms (e.g. unstable or untreated sleep apnea)
• Presence of intramural thrombus, tumor or other abnormality or condition that precludes vascular access, or manipulation of the catheter
• Life expectancy or other disease processes likely to limit survival to less than 12 months
• Acute Covid-19 infection (fever and/or biological inflammatory syndrome, and positive test documented)

Lab values

• Chronic severe Heart Failure (NYHA functional class IV and/or LVEF \< 25%)

Other

• First AF ablation procedure indication was persistent AF lasting longer than 24 months
• Severe obesity (BMI \> 50)
• Very dilated Left Atrium (LA) (e.g. LA diameter \> 55 mm and/or LA surface \> 40 cm2 determined by 2D echocardiography)
• Patients with AF secondary to an obvious reversible cause
• Inadequate anticoagulation as defined in the inclusion criteria
• Contraindications to anticoagulation (heparin, warfarin or NOAC)
• Patients who are or may potentially be pregnant
• Patient diagnosed with hypertrophic cardiomyopathy
• Documented arterial thromboembolic event (including TIA) within the past 12 months (365 days)
• Diagnosed atrial myxoma
• Significant congenital anomaly or medical problem that in the opinion of the investigator would preclude enrollment

• Patients 21 years of age or older indicated for redo AF ablation
• Previous catheter or surgical ablation for paroxysmal AF, persistent AF, or long-standing persistent AF
• Documented symptomatic AF recurrences that occurred within the last 12 months and persisted beyond 3 months after the last AF ablation procedure
• Continuous anticoagulation with warfarin (INR 2-3) or NOAC for \> 4 weeks prior to ablation
• Patients must be able and willing to provide written informed consent to participate in the clinical trial