Atrial Fibrillation Prevention in Post Coronary Artery Bypass Graft Surgery With Cryoablation for Ganglionic Plexi
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ClinicalTrials.gov Identifier: NCT02035163 |
Recruitment Status :
Recruiting
First Posted : January 14, 2014
Last Update Posted : April 5, 2019
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Atrial fibrillation after coronary artery bypass graft is a common complication.
The investigators have thought that the mechanism of temporarily postoperative atrial fibrillation is closely related to the autonomic nervous system imbalance.
In a last several years, cryoablation was substituted for atrial incision in many reports to simplify the maze procedure.
However, there has been no comparative study to delineate the feasibility of the use of cryoablation.
Condition or disease | Intervention/treatment | Phase |
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Complication of Coronary Artery Bypass Graft Atrial Fibrillation | Procedure: Two sites cryoablation | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 62 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Single (Participant) |
Primary Purpose: | Treatment |
Official Title: | Atrial Fibrillation Prevention in Post Coronary Artery Bypass Graft Surgery With Cryoablation for Ganglionic Plexi |
Study Start Date : | July 2012 |
Estimated Primary Completion Date : | December 2019 |
Estimated Study Completion Date : | December 2019 |

Arm | Intervention/treatment |
---|---|
Active Comparator: Two sites cryoablation group
Two ganglionic plexi around atrium was performed with 90-second cryoablation.
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Procedure: Two sites cryoablation
Two ganglionic plexi around atrium was performed with 90-second cryoablation. |
No Intervention: Control group
No Intervention group
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- freedom of atrial fibrillation or other atrial arrhythmia [ Time Frame: 5 days after surgery ]check the occurrence of atrial fibrillation through EKG monitoring And bradycardia(<40/min) or tachycardia(>110/min) does not occur

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- coronary artery graft bypass patient
- sinus rhythm
Exclusion Criteria:
- Patients using antiarrhythmic
- severe hypotension after surgery ( systolic blood pressure <90mmHg)
- history of atrial fibrillation

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02035163
Contact: Sung Hwan Kim, MD | 82-10-9109-8957 | sunghwan@catholic.ac.kr |
Korea, Republic of | |
The Catholic University of Korea, Seoul St Mary's Hospital | Recruiting |
Seoul, Seo Cho Gu, Korea, Republic of, 137-701 | |
Contact: Sung Hwan Kim, MD 82-10-9109-8957 sunghwan@catholic.ac.kr |
Study Chair: | Yong Seog Oh, Ph.D | Seoul St. Mary's Hospital |
Responsible Party: | Yong Seog Oh, MD, Seoul St. Mary's Hospital |
ClinicalTrials.gov Identifier: | NCT02035163 |
Other Study ID Numbers: |
APIP |
First Posted: | January 14, 2014 Key Record Dates |
Last Update Posted: | April 5, 2019 |
Last Verified: | April 2019 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Atrial fibrillation coronary artery bypass graft cryoablation ganglionic plexi |
Atrial Fibrillation Arrhythmias, Cardiac Heart Diseases Cardiovascular Diseases Pathologic Processes |