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Clinical Trials in China / NCT07057713
Starting soon Not applicable

Total Arterial vs. Mixed Grafting in Left Coronary CABG

NCT07057713 · tracked via the Priya Life Science China tracker
Sponsor
Second Hospital of Jilin University
Phase
Not applicable
Started
2026-08-01
Last updated
2026-04-23

Condition(s) studied

Coronary Artery DiseaseCoronary Artery Bypass GraftingArterial GraftGraft PatencyMajor Adverse Cardiovascular Events

Investigational drug(s) / intervention(s)

Total Arterial GraftingConventional Mixed Grafting

Total Arterial Grafting: Coronary artery bypass grafting using only arterial conduits in the left coronary artery system. The left internal thoracic artery (LITA) is grafted to the LAD, and the radial artery is anastomosed to the obtuse marginal or diagonal branches. This approach avoids the use of saphenous vein grafts for the left coronary system.

Conventional Mixed Grafting: A standard coronary artery bypass grafting (CABG) procedure where the left internal thoracic artery (LITA) is grafted to the LAD, and saphenous vein grafts are used for the obtuse marginal or diagonal branches of the left coronary system. This approach represents the conventional mixed arterial-venous strategy.

Study summary

This is a prospective, randomized, double-blind controlled trial comparing the clinical efficacy of total arterial grafting (internal thoracic artery and radial artery) versus conventional mixed grafting (internal thoracic artery and great saphenous vein) in the left coronary artery system during coronary artery bypass grafting (CABG). A total of 400 patients undergoing elective CABG at the Second Hospital of Jilin University will be enrolled and randomized into two groups. The primary endpoint is graft patency at 12 months postoperatively, evaluated by coronary angiography or CT angiography. Secondary outcomes include perioperative complications, major adverse cardiovascular events (MACE), and long-term clinical prognosis. The study aims to provide evidence-based guidance on optimal graft selection in CABG.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age ≥ 18 years 2. Diagnosed with multivessel coronary artery disease 3. Indicated for elective coronary artery bypass grafting (CABG) involving ≥3 coronary vessels 4. Right coronary artery stenosis \>75% 5. Able and willing to provide written informed consent Exclusion Criteria: 1. Scheduled for concurrent cardiac procedures (e.g., valve surgery, congenital heart disease repair, aortic dissection surgery, atrial fibrillation ablation) 2. Severe stenosis of left or right subclavian artery 3. Unsuitable saphenous veins (e.g., bilateral varicosities) 4. Unsuitable radial artery as assessed preoperatively 5. History of intracranial hemorrhage or ischemic stroke within the past 14 days 6. Severe hepatic or renal insufficiency 7. Acute myocardial infarction within 72 hours prior to surgery 8. History of prior CABG or other cardiac surgery

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The Second Hospital of Jilin University Changchun Jilin

More Second Hospital of Jilin University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07057713 on ClinicalTrials.gov ↗ ← All trials in China