Atrial Fibrillation Clinical Trial
Official title:
Atrial Fibrillation Treatment Using Laser Ablation of Cardiac Tissue During Concomitant Cardiac Surgery
The purpose of study is to conduct a pivotal evaluation of the EndoPhotonix™ SOLAR™ System
and ATRILAZE™ System in order to obtain a labeling claim on the devices for the treatment of
atrial fibrillation.
The study will test the safety and effectiveness of the EndoPhotonix™ Laser Ablation Systems
to photocoagulate cardiac tissue during cardiac surgery, to create electrical isolation of
the pulmonary veins and create other electrical isolation lesions in order to treat atrial
fibrillation. The surgical procedure will be conducted during concomitant mitral valve
repair or replacement surgery or in combination with other cardiac surgery including aortic
valve surgery, tricuspid valve surgery, or coronary artery bypass surgery.
The study objective is to generate Level II controlled data to support the expansion of indications for the SOLAR™ System based on 0-30 day data; as well as to support the expansion of indications for the SOLAR™ System and ATRILAZE™ System for the treatment of atrial fibrillation based on 180 days data. The data will be evaluated by comparing post-operative data to the historical control data. The subjects in the study cohort will receive laser ablation therapy using the investigational device during a concomitant surgical procedure. ;
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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