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Maximum Targeted Ablation of Atrial Flutter

Primary Purpose

Atrial Flutter

Status
Unknown status
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
radiofrequency catheter ablation
Sponsored by
Lawson Health Research Institute
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Flutter focused on measuring atrial flutter, ablation, voltage targeted

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • London Health Sciences CenterRecruiting

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
June 21, 2007
Last Updated
June 21, 2007
Sponsor
Lawson Health Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT00491010
Brief Title
Maximum Targeted Ablation of Atrial Flutter
Official Title
Maximum Targeted Ablation of Atrial Flutter
Study Type
Interventional

2. Study Status

Record Verification Date
June 2007
Overall Recruitment Status
Unknown status
Study Start Date
July 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
February 2008 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Lawson Health Research Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Flutter
Keywords
atrial flutter, ablation, voltage targeted

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
radiofrequency catheter ablation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Allan Skanes, MD
Phone
519-685-8500
Ext
32739
Email
askanes@uwo.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Lorne gula, MD
Phone
519 685-8500
Ext
32739
Email
lgula@uwo.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Allan c Skanes, MD
Organizational Affiliation
University of Western Ontario, London Health Sciences Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
London Health Sciences Center
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5A5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lorne Gula, MD

12. IPD Sharing Statement

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Maximum Targeted Ablation of Atrial Flutter

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