Arrhythmias Clinical Trial
Official title:
Comparative Study of Two 3D Electroanatomical Mapping Systems for Ablations of Different Complex Arrhythmias
Verified date | April 2017 |
Source | Rabin Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Three dimensional anatomical mapping is an established method facilitating ablation of cardiac arrhythmias. The most commonly used systems are CARTO® System (Biosense Webster, Inc., Diamond Bar, CA, USA) and EnSite NavX™ (St. Jude Medical, Inc., St. Paul, MN, USA). These two systems has been compared in only a few studies. Recent technical advances resulted in the development of new versions of both systems. To the best of the investigators knowledge no studies have been performed for direct comparison of the newer versions of these two systems. The aim of the study to compare two systems for the use in the ablation of complex arrhythmias.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | October 2016 |
Est. primary completion date | July 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: 1. Age 18- 80. 2. Ability to sign informed consent. 3. History of one of the following arrhythmias requiring the use of 3D electroanatomical mapping: - Symptomatic paroxysmal or persistent atrial fibrillation with failed treatment of at least two anti-arrhythmic drugs. - Ischemic ventricular tachycardia necessitating ablation as per decision of electrophysiologist. - Symptomatic atrial tachycardia after failed medical treatment. - Symptomatic idiopathic ventricular tachycardia. Exclusion Criteria: 1. Unstable patients not allowing performing procedure more than 2 hours 2. Patients planned for one of the two systems compared for whatever reason Ex. procedure planned with NAVX system Array Balloon). |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Rabin Medical Center |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Procedure duration | Average procedure duration (needle to catheters withdrawal) | Procedure duration - average expected 2.5 hours | |
Secondary | Fluoroscopy time | Average fluro time in each of groups. | Procedures will be evaluated for the fluoro time, expected average 30 min | |
Secondary | Procedure success | Recurrency of the arrhythmia assessed by blinded electrophysiologist | Patients will be followed for one year for recurrency of arrhythmia |
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