Discerning Symptomatic and Asymptomatic Episodes Pre and Post Radiofrequency Ablation of Atrial Fibrillation

NACompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

September 30, 2008

Primary Completion Date

April 30, 2014

Study Completion Date

December 31, 2014

Conditions
Atrial Fibrillation
Interventions
DEVICE

Implantable Loop Recorder (ILR)

Insertion of ILR 3 months prior to clinical ablation procedure to collect data on actual Atrial Fibrillation episodes and correlation with patient symptoms through patient diary entry. Then patient undergoes their previously indicated clinical ablation procedure and is then followed up with ILR insitu for 30 months post-ablation for the same as mentioned above.

Trial Locations (8)

V8R 4R2

Victoria Cardiac Arrhythmia Trials Inc., Victoria

B3H 3A7

QEII Health Sciences Centre, Halifax

L8L 2X2

Hamilton Health Sciences Centre, Hamilton

N6A 4G5

London Health Sciences Centre, London

L3Y 2P9

Southlake Regional Health Centre, Newmarket

K1Y 4W7

University of Ottawa Heart Institute, Ottawa

H3G 1A4

Hôpital Général de Montréal-McGill, Montreal

G1V 4G5

Hôpital Laval, Québec

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Medtronic

INDUSTRY

lead

Ottawa Heart Institute Research Corporation

OTHER