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Sponsored by: |
Lawson Health Research Institute |
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Information provided by: | Lawson Health Research Institute |
ClinicalTrials.gov Identifier: | NCT00491010 |
Patients undergoing atrial flutter ablation will be randomized to either the standard ablation approach or voltage targeted approach. Patients will be followed for one year to assess outcome of the ablation technique
Condition | Intervention | Phase |
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Atrial Flutter |
Procedure: radiofrequency catheter ablation |
Phase IV |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Single Blind, Active Control, Parallel Assignment, Safety/Efficacy Study |
Official Title: | Maximum Targeted Ablation of Atrial Flutter |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Allan Skanes, MD | 519-685-8500 ext 32739 | askanes@uwo.ca |
Contact: Lorne gula, MD | 519 685-8500 ext 32739 | lgula@uwo.ca |
Canada, Ontario | |
London Health Sciences Center | Recruiting |
London, Ontario, Canada, N6A 5A5 | |
Sub-Investigator: Lorne Gula, MD |
Principal Investigator: | Allan c Skanes, MD | University of Western Ontario, London Health Sciences Center |
Study ID Numbers: | R-06-153, 12266 |
Study First Received: | June 21, 2007 |
Last Updated: | June 21, 2007 |
ClinicalTrials.gov Identifier: | NCT00491010 |
Health Authority: | Canada: Ethics Review Committee |
atrial flutter ablation voltage targeted |
Heart Diseases Atrial Flutter Arrhythmias, Cardiac |
Pathologic Processes Cardiovascular Diseases |