MedPath

Maximum Targeted Ablation of Atrial Flutter

Phase 4
Conditions
Atrial Flutter
Registration Number
NCT00491010
Lead Sponsor
Lawson Health Research Institute
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

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
Not specified
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

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

London Health Sciences Center

🇨🇦

London, Ontario, Canada

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