Clinical Trial Search

Primary: Occurrence of Post-operative Atrial Fibrillation Requiring Treatment After Open Heart Surgery — 50; 56; 58; 48 Participants

Primary: Postoperative Atrial Fibrillation — 27.2; 27.8; 25.9 percentage of patients — p=0.95

Primary: Incidence of Atrial Fibrillation Requiring Treatment — 9; 21 participants — p=0.02

Primary: Total Number of Days in Hospital — 5.1; 5.0 days — p=0.76

Primary: Any First Post-op Atrial Fibrillation or Flutter (AF) — 233; 227 Participants

Primary: Incidence of Atrial Fibrillation — 6; 16 participants — p=0.02

Primary: Atrial Fibrillation — 6; 1 participants

Primary: Number of Participants With Strokes — 0; 0 participants — p=1.0

Primary: Primary Safety Endpoint — 3.9; 3.6 percentage of participants

Primary: Number of Participants With New Episodes of Atrial Fibrillation — 12; 27 participants

Primary: Number of Participants With Adverse Events — 0; 0 Participants

Primary: Numbers of Participants Free From AF — 20; 96; 20; 97 Participants

Primary: Incidence of Documented Post-operative Atrial Fibrillation — 17; 2 Participants

Primary: Time to In-hospital Post-operative Atrial Fibrillation (POAF) — 224.38; 194.76 hours — p=0.18

Primary: Incidence of Postoperative Atrial Fibrillation — 5; 4; 5 participants

Primary: Atrial Fibrillation Incidence After Open Cardiac Valve Repair — 6; 13 participants

Primary: Postoperative Length of Stay — 8; 7 days

Primary: Procedure Time (Minutes) — 128.7; 137.8 minutes

Primary: Number of Participants Who Developed Postoperative Atrial Fibrillation — 33; 30 participants — p=<0.01

Primary: Primary Safety Endpoint — 0; 0; 4.2; 0 percentage of participants

Primary: Number of Participants With Postoperative Atrial Fibrillation — 39; 33 Participants

Primary: The Number of Participants With Atrial Fibrillation — 26; 37 Participants

Primary: Clinically Significant Atrial Fibrillation — 5; 6 Participants

Primary: Number of Patients With at Least One Inappropriate MAI Criterion — 61; 11; 17 participants

Primary: All Hospital Episodes (Emergency Room or Patient Request for OPD) Related to Treatment for Atrial Arrhythmia — 19; 76; 23 Participants — p=<0.0001

Primary: Subjects Achieving Normal Sinus Rhythm (NSR) in Patients With Paroxysmal AF — 0; 2; 0; 0 Participants

Primary: Percentage of Subjects Without Symptoms of Atrial Fibrillation at 3 Months — 95; 93.5 Percentage of subjects — p=0.75

Primary: Number of Perioperative Complications Associated With AtriClip Placement — 0 perioperative complications reported

Primary: The Number of Patients in Sinus Rhythm at 12 Months. — 12 Participants

Primary: Number of Participants With Transient Ischemic Attack — 6; 22 participants — p=0.001