Safety and Efficacy Study of The Combined Ablation Procedure To Treat Longstanding Persistent Atrial Fibrillation



Status:Archived
Conditions:Atrial Fibrillation
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:Any
Updated:7/1/2011
Start Date:April 2010
End Date:April 2013

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Trial Summary
Trial Overview
Inclusion Criteria

Feasibility Study For Safety and Efficacy Evaluation Of The Combined Ablation Procedure For The Treatment Of LongStanding Persistent Atrial Fibrillation


This is a multi-center, prospective open label, feasibility study evaluating the safety and
efficacy of the combined ablation procedure for the treatment of longstanding persistent
atrial fibrillation.


The purpose of this feasibility study is to evaluate the safety and efficacy of the
epicardial / endocardial combined procedure using the nContact Numeris®-AF Guided
Coagulation System with VisiTrax® epicardially and the St. Jude Medical Therapy™ Cool Path™
Ablation Catheter endocardially to treat longstanding persistent Atrial Fibrillation (AF)
patients.


We found this trial at
4
sites
Texas Cardiac Arrhythmia
Austin, Texas 78705
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Austin, TX
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The Care Group, St Vincent Hospital
Indianapolis, Indiana 46250
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Indianapolis, IN
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Baptist Memorial Hospital
Memphis, Tennessee 38120
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Memphis, TN
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Cardiothoracic Surgical Associates, CJW Medical Center
Richmond, Virginia 23225
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Richmond, VA
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