European CURE-AF Study

NACompletedINTERVENTIONAL
Enrollment

26

Participants

Timeline

Start Date

June 19, 2008

Primary Completion Date

February 28, 2011

Study Completion Date

July 10, 2013

Conditions
Atrial Fibrillation
Interventions
DEVICE

Cardioblate surgical ablation system

This investigation is a prospective, non-randomized multicenter clinical trial evaluating the outcome of patients with AF requiring concomitant open heart surgery plus the Cardioblate Surgical Ablation System using the modified Maze III procedure. The trial population includes patients requiring valve replacements or repairs, atrial septal defect (ASD) repairs, patent foramen ovale (PFO) closure or coronary artery bypass grafts (CABG) procedures.

PROCEDURE

Surgical RF Ablation

This investigation is a prospective, nonrandomized multicenter clinical trial evaluating the outcome of patients with AF requiring concomitant open heart surgery plus the Cardioblate Surgical Ablation System using the modified Maze III procedure. The trial population includes patients requiring valve replacements or repairs, atrial septal defect (ASD) repairs, patent foramen ovale (PFO) closure or coronary artery bypass grafts (CABG) procedures.

Trial Locations (5)

5021

Haukeland University Hospital - Department of Cardiothoracic Surgery, Bergen

7018

St. Elizabeth Heart Center - Department of Cardiothoracic Surgery, Trondheim

61231

Kerckhoff Clinic - Department of Thoracic & Cardiovascular Surgery, Bad Nauheim

03048

Heart Center Cottbus - Department of Cardiac Surgery, Cottbus

02-097

Public Central Teaching Hospital - Department of Cardiac Surgery, Warsaw

Sponsors
All Listed Sponsors
lead

Medtronic Cardiovascular

INDUSTRY

NCT04645615 - European CURE-AF Study | Biotech Hunter | Biotech Hunter