NCT Number: NCT01772030
Atrial Fibrillation Recurrence After Cryoballoon Ablation
The purpose of the study is to evaluate the mechanisms of recurrent atrial fibrillation after cryoballoon ablation using the Arctic Front Ablation System. For those with pulmonary vein reconnection, specific sites of reconnection will be evaluated with left atrial intracardiac echo (ICE) guidance. The Achieve mapping catheter will be evaluated head-to-head with our current method of ICE-guided recordings from a conventional mapping catheter with high output pulmonary venous pacing.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
UPMC Passavant, Pittsburgh, Pennsylvania, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Patients undergoing re-do catheter ablation procedure after index procedure with cryoballoon ablation
- At least 18 years old
- Able to read and understand informed consent
Exclusion criteria
- Unable to give informed consent
Treatment and study plan
Primary outcomes
-
Presence or absence of pulmonary vein isolation or reconnection
Time frame: During repeat cryoballoon ablation procedure
Sponsors and collaborators
Lead sponsor
University of Pittsburgh
Other
Collaborators
- Medtronic
Registry information
Official study title
Mechanisms and Patterns of Atrial Fibrillation Recurrence After Cryoballoon Ablation
Important dates
- Study start
- 2013
- Primary completion
- 2019
- Study completion
- 2019
- First posted
- Jan 21, 2013
- Registry last updated
- Feb 12, 2020
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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