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Clinical Trial Summary

To compare of atrial arrhythmia incidence in patients with coronary artery disease and atrial fibrillation history, undergoing either coronary artery bypass grafting plus temporary spinal cord stimulation or coronary artery bypass grafting alone


Clinical Trial Description

The study includes 60 patients. Patients are randomized into 2 groups: coronary artery bypass grafting plus b-blocker treatment (according to guidelines; group I) and coronary artery bypass grafting plus b-blocker treatment (according to guidelines) plus temporary spinal cord stimulation (group 2). Temporary spinal cord stimulation is performed for 3 days before surgery and 7 days after coronary artery bypass grafting. Continuous ECG during intensive care unit stay, daily ECG and 24-h Holter monitor recordings at 7, 14, 21, and 30 days after coronary artery bypass grafting, external loop recorder after discharge from intensive care unit until 30 days after coronary artery bypass grafting. Rhythm status and clinical outcome assessment at 12 month follow up ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03539354
Study type Interventional
Source Meshalkin Research Institute of Pathology of Circulation
Contact Alexander B Romanov, PhD
Phone +79137172652
Email abromanov@mail.ru
Status Recruiting
Phase N/A
Start date July 1, 2018
Completion date May 2020

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