Status:
WITHDRAWN
Comparison of External Event Recorders for Atrial Fibrillation Monitoring
Lead Sponsor:
Dhanunjaya Lakkireddy, MD, FACC
Conditions:
Atrial Fibrillation
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Ablation of atrial fibrillation is a well established treatment method to restore normal sinus rhythm and eliminate the need for continued antiarrhythmic therapy and anticoagulation. Absence of sympto...
Eligibility Criteria
Inclusion
- All subjects who undergo radiofrequency ablation of paroxysmal AF.
Exclusion
- Subjects with known allergy to sticky patches of event monitor
- Subjects with skin infection or other problems on the chest that interferes with monitor implantation
- Subjects who are scheduled for radiation therapy
- Subjects who are scheduled for therapeutic ultrasound (like lithotripsy)
- Subjects who are scheduled for MRI
- Subjects who are scheduled for a procedure that uses diathermy.
- Subjects, in the opinion of the investigator, are not suitable candidates for the study
- Subjects that do not have analog telephone line at home.
- Existing Cardiac Rhythm Management Device (e.g., pacemaker or ICD)
Key Trial Info
Start Date :
January 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2012
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00863382
Start Date
January 1 2009
End Date
January 1 2012
Last Update
May 7 2012
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
University of Kansas Medical Center
Kansas City, Kansas, United States, 66160