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Prophylactic Maze to Prevent Atrial Fibrillation in Adult Cardiac Surgery — PREVENT-AF  

Coronary Artery Disease Clinical Trial

Official title:
Prophylactic Limited Left Sided Maze Procedure to Prevent Post-operative Atrial Fibrillation in Adult Cardiac Surgery Patients

Clinical Trial Summary

This study will look at performing a prophylactic limited left sided maze procedure during concomitant adult cardiac surgery to prevent the common occurrence of postoperative atrial fibrillation.

Clinical Trial Description

This is a prospective, single site, randomized, small feasibility study using a FDA approved device for a new indication. Subjects undergoing a CABG, AVR, or CABG/AVR will be randomized 1 to 1 to a control or treatment group. The control group will undergo their index cardiac surgery procedure only. The treatment group will undergo their index cardiac procedure along with a limited left sided maze procedure. The maze procedure will be done with the Atricure synergy ablation system. This is an FDA approved device that will be used for this new indication. The left sided limited maze procedure will consist of pulmonary vein isolation and removal of the left atrial appendage. A total of 60 subjects will be enrolled in this study at a single site. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03604432
Study type Interventional
Source Spectrum Health Hospitals
Contact
Status Completed
Phase N/A
Start date February 1, 2020
Completion date February 10, 2023
View Details
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