Long-Term Follow-Up of Patients Undergoing Catheter Ablation

This study is currently recruiting participants.
Verified March 2011 by University of Oklahoma
Sponsor:
Information provided by:
University of Oklahoma
ClinicalTrials.gov Identifier:
NCT00584558
First received: December 20, 2007
Last updated: March 2, 2011
Last verified: March 2011

December 20, 2007
March 2, 2011
December 2000
November 2050   (final data collection date for primary outcome measure)
Arrhythmia recurrence [ Time Frame: 0-10 years ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00584558 on ClinicalTrials.gov Archive Site
Complications [ Time Frame: 0-10 years ] [ Designated as safety issue: Yes ]
Same as current
Not Provided
Not Provided
 
Long-Term Follow-Up of Patients Undergoing Catheter Ablation
Long-Term Follow-Up of Patients Undergoing Catheter Ablation

The purpose of this study is to assess the long-term effects of catheter ablation procedures performed at the OU Medical Center.

The purpose of this study is to assess the long-term effects of catheter ablation procedures performed at this institution, including recurrence of the ablated arrhythmia and any late complications.

Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample

Patients undergoing catheter ablation at the OU Medical Center

Arrhythmia
Procedure: Catheter Ablation
Catheter Ablation of arrhythmias
Other Names:
  • All approved ablation catheters
  • Investigational ablation catheters
1
Patients undergoing catheter ablation.
Intervention: Procedure: Catheter Ablation
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
5000
November 2050
November 2050   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Undergoing catheter ablation at the OU Medical Center

Exclusion Criteria:

  • Prisoners
  • Refusal to participate
Both
18 Years and older
No
Contact: Karen Beckman, MD 405-271-9696 ext 37536 Karen-Beckman@ouhsc.edu
United States
 
NCT00584558
09343
No
Karen Beckman, M.D., University of Oklahoma Health Science Center
University of Oklahoma
Not Provided
Principal Investigator: Karen Beckman, MD University of Oklahoma
University of Oklahoma
March 2011

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