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CARTO® 3 System and Real Time Intracardiac Ultrasound — IUAF  

Atrial Fibrillation Clinical Trial

Official title:
CARTO® 3 System and Real Time Intracardiac Ultrasound for Ablation of Drug Refractory Recurrent Symptomatic Paroxysmal AF: Acute Procedural Outcomes Study

Clinical Trial Summary

This is a prospective, multicenter, non-randomized observational study of subjects 18 years and older undergoing RF ablation with drug refractory recurrent symptomatic paroxysmal Atrial Fibrillation (AF).

Clinical Trial Description

This study is purposed to measure "real world" acute procedural outcomes (procedural efficiency and acute safety) associated with use of the CARTO® 3 System and real time intracardiac ultrasound in a clinical setting in subjects with drug refractory recurrent symptomatic paroxysmal AF. ;

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01716663
Study type Observational
Source Biosense Webster, Inc.
Contact
Status Completed
Phase N/A
Start date October 2012
Completion date September 2013
View Details
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