Recruiting

Atrial Flutter

Sponsor:

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Code:

NCT00491010

Conditions

Atrial Flutter

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

radiofrequency catheter ablation

Study Details

Brief summary:

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

Conditions

Atrial Flutter

Study ID

NCT00491010

Start date

Jul, 2006

Status verified date

Jun, 2007

Completion date

Feb, 2008

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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

Study Design

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Interventions

radiofrequency catheter ablation

Central Contacts and Locations

Central contacts

Allan Skanes, MD

519-685-8500askanes@uwo.ca

Lorne gula, MD

519 685-8500lgula@uwo.ca

Locations

London Health Sciences Center

Recruiting

London, Ontario, Canada, N6A 5A5

More Information

Sponsor

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Last update posted

Jun 25, 2007

Last verified

Jun, 2007

Keywords

  • atrial flutter
  • ablation
  • voltage targeted

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's on 2007-06-25.