The purpose of this study is to test the safety and efficacy of the Epicor LP Cardiac Ablation System for treating permanent atrial fibrillation during concomitant open chest and/or open heart surgery for one of more of the following procedures: mitral valve repair or replacement, aortic valve repair or replacement, tricuspid valve repair or replacement, coronary artery bypass surgery or patent foramen ovale (PFO closure).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
112
Surgical ablation of permanent AF during concomitant open chest and/or open heart surgery
Concomitant AF ablation during mitral valve surgery
St. Agnes Medical Center
Fresno, California, United States
Manatee Memorial Hospital
Bradenton, Florida, United States
Freedom From Atrial Fibrillation in the Absence of Any AF Therapies
Freedom from atrial fibrillation (AF) at 6 months in absence of any AF therapies.
Time frame: 6 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Blake Medical Center
Bradenton, Florida, United States
Cardiology Consultants, MD's PA (Baptist Hospital)
Pensacola, Florida, United States
NorthShore University Health System
Evanston, Illinois, United States
Community Hospital
Munster, Indiana, United States
Midatlanatic Cardiovascular Associates, PA; Union Memorial Hospital
Baltimore, Maryland, United States
William Beaumont Hospital
Royal Oak, Michigan, United States
Minneapolis Heart Institute Foundation/Abbott NW Hospital
Minneapolis, Minnesota, United States
HealthEast St. Joseph's Hospital
Saint Paul, Minnesota, United States
...and 5 more locations