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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02035163
Other study ID # APIP
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date July 2012
Est. completion date December 2019

Study information

Verified date April 2024
Source Seoul St. Mary's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

Modified maze procedures that use energy sources for the ablation of atrial fibrillation concomitant with cardiac surgery have been shown to improve outcomes in patients with atrial fibrillation. Cryoablation of atrial fibrillation recently has been shown to lead to outcomes that were at least equivalent to those reported for other energy modalities over both short- and medium-term follow-up times.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2019
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Two sites cryoablation
Two ganglionic plexi around atrium was performed with 90-second cryoablation.

Locations

Country Name City State
Korea, Republic of The Catholic University of Korea, Seoul St Mary's Hospital Seoul Seo Cho Gu

Sponsors (1)

Lead Sponsor Collaborator
Yong Seog Oh

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary freedom of atrial fibrillation or other atrial arrhythmia check the occurrence of atrial fibrillation through EKG monitoring And bradycardia(<40/min) or tachycardia(>110/min) does not occur 5 days after surgery
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