IMPULSE: A Safety and Feasibility Study of the IOWA Approach Endocardial Ablation System to Treat Atrial Fibrillation

Inclusion Criteria

• Patients with PAF who have had at least one AF episode documented within one (1) year prior to enrollment. Documentation may include ECG, transtelephonic monitor (TTM), Holter monitor (HM), or telemetry strip.
• Patients who have failed at least one antiarrhythmic drug (AAD; class I or III, or AV nodal blocking agents such as beta blockers and calcium channel blockers) as shown by recurrent symptomatic AF, or intolerance to the AAD or AV nodal blocking agents.
• Patients who are ≥ 18 and ≤ 70 years of age on the day of enrollment.
• Antero-posterior left atrial diameter ≤ 5.5 cm as documented by transthoracic echocardiography (TTE) or computed tomography (CT) within 3 months prior to the procedure.
• Subject has no contraindications to intraoperative transesophageal echocardiography;
• Left ventricular ejection fraction ≥40% as documented by TTE within 12 months prior to the procedure.
• Received a standard cardiac work up and is an appropriate candidate for an investigational procedure as determined by study investigators.
• Subject is willing and capable of providing Informed Consent to undergo study procedures and participate in all examinations and follow-up visits and tests associated with this clinical study.

Exclusion Criteria

• Patients on amiodarone at any time during the past 3 months prior to enrollment.
• AF secondary to electrolyte imbalance, thyroid disease, or reversible or non-cardiac cause.
• AF episodes lasting > 7 days.
• Previous ablation for AF.
• Patient has a prosthetic heart valve.
• Patient has a left atrial appendage device
• Prior history of pericarditis or pericarditis within 3 months based on the TTE examination.
• Subject is a woman of child bearing age
• Prior history of rheumatic fever.
• Prior history of medical procedure involving instrumentation of the left atrium (previous ablation, Atrial septal defect ASD closure, left atrial appendage occlusion)
• History of severe chronic gastrointestinal problems involving the esophagus, stomach and/or untreated acid reflux
• History of abnormal bleeding and/or clotting disorder.
• Active malignancy or history of treated cancer within 24 months of enrollment.
• Clinically significant infection or sepsis.
• History of stroke or TIA within prior 6 months
• New York heart Association (NYHA) class IIIb or IV congestive heart failure and/or any heart failure hospitalization within 3 months prior to enrollment.
• Body mass index > 35.
• Estimate glomerular filtration rate (eGFR) 50 mm Hg, severe Chronic Obstructive Pulmonary Disease or restrictive lung disease.
• Patients with any other significant uncontrolled or unstable medical condition (such as uncontrolled brady-arrhythmias, ventricular arrhythmias, hyperthyroidism or significant coagulation disorder).
• Life expectancy less than one year.
• Clinically significant psychological condition that in the physician's opinion would prohibit the subject's ability to meet the protocol requirements.
• History of blood clotting or bleeding abnormalities.
• Contraindication to anticoagulation (i.e., heparin, dabigatran, Vitamin K Antagonists such as warfarin).
• Enrolled in another cardiac clinical study that would interfere with this study.