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Concomitant Treatment of Permanent Atrial Fibrillation


A Prospective, Multi-center Study With Case Matched Controls to Evaluate the Safety and Efficacy of the AtriCure Bipolar System for the Treatment of Continuous Atrial Fibrillation as Adjunct Therapy to Elective Open Heart Surgery




RESTORE-SR study is a multi-center, prospective, nonrandomized study with case matched concurrent controls to evaluate the safety and efficacy of the AtriCure Bipolar System

Study Status: Completed


Condition Intervention Phase
Atrial Fibrillation Device: Surgical bipolar radiofrequency ablation using the AtriCure Bipolar System Phase 3

Verified by AtriCure, Inc. January, 2012

Sponsored by: AtriCure, Inc.
Information provided by: AtriCure, Inc. identifier: NCT00566787

Study Type: Interventional

Study Design: Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Cleveland Clinic
Cleveland, Ohio 44195
United States

A. Marc Gillinov, MD., Principal Investigator

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