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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01008722
Other study ID # 684
Secondary ID R01HL083359
Status Recruiting
Phase N/A
First received November 5, 2009
Last updated December 10, 2013
Start date June 2009
Est. completion date May 2014

Study information

Verified date December 2013
Source University of California, San Diego
Contact Sanjiv M. Narayan, MD, PhD
Phone (858) 642-1108
Email snarayan@ucsd.edu
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

The study is conducted in patients with atrial fibrillation undergoing clinically prescribed ablation. The study hypothesis is that ablation at specific sites that are identified to 'drive' the atrial fibrillation may improve the success of the ablation procedure.


Recruitment information / eligibility

Status Recruiting
Enrollment 98
Est. completion date May 2014
Est. primary completion date April 2014
Accepts healthy volunteers No
Gender Both
Age group 21 Years to 80 Years
Eligibility Inclusion Criteria:

- Subjects will be patients undergoing electrophysiology study and ablation for paroxysmal or persistent atrial fibrillation (AF) after having failed >or= 1 anti-arrhythmic drug.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of California, San Diego La Jolla California
United States VA San Diego Medical Center San Diego California

Sponsors (2)

Lead Sponsor Collaborator
University of California, San Diego National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survival Free of Atrial Fibrillation 6 months No
Secondary Termination of atrial fibrillation during ablation acute No
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