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Clinical Trial Summary

The aims of study are (1) to compare early and 1-year graft patency rates in patients who underwent coronary artery bypass grafting (CABG) based on conventional coronary angiography(CAG) versus cardiac computed tomography(CT)-derived fractional flow reserve(FFR), and (2) to demonstrate difference in clinical outcomes between the 2 groups.


Clinical Trial Description

The CABG-COREA trial is designed as a randomized, controlled trial to recruit 96 patients who undergo coronary artery bypass grafting. Patients were randomized by use of a randomization table. Coronary arteries are revascularized based on conventional coronary angiography or cardiac computed tomography-derived fractional flow reserve according to the randomization result. The primary end point is to evaluate early and 1-year postoperative graft patency. The secondary end points are overall survival, freedom from cardiac death and freedom from MACCE(major adverse cardiac or cerebrovascular events). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06028165
Study type Interventional
Source Myongji Hospital
Contact Min-Seok Kim, MD, PhD, MSc
Phone 82-10-8482-0380
Email minseok.kim.md.phd@gmail.com
Status Recruiting
Phase N/A
Start date October 20, 2023
Completion date October 1, 2025

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