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Maximum Targeted Ablation of Atrial Flutter

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified June 2007 by Lawson Health Research Institute.
Recruitment status was:  Recruiting
Sponsor:
Information provided by:
Lawson Health Research Institute
ClinicalTrials.gov Identifier:
NCT00491010
First received: June 21, 2007
Last updated: NA
Last verified: June 2007
History: No changes posted

June 21, 2007
June 21, 2007
July 2006
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No Changes Posted
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Maximum Targeted Ablation of Atrial Flutter
Maximum Targeted Ablation of Atrial Flutter
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
Not Provided
Interventional
Phase 4
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind
Primary Purpose: Treatment
Atrial Flutter
Procedure: radiofrequency catheter ablation
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Unknown status
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February 2008
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Inclusion Criteria:

  • patients undergoing TV-IVC isthmus ablatin for atrial flutter

Exclusion Criteria:

  • atypical atrial flutter
  • <18 years old any atrial surgery or pacemaker refusal to participate
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Canada
 
 
NCT00491010
R-06-153
12266
No
Not Provided
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Lawson Health Research Institute
Not Provided
Principal Investigator: Allan c Skanes, MD University of Western Ontario, London Health Sciences Center
Lawson Health Research Institute
June 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP