Radial Artery Versus No-touch Saphenous Vein
Coronary Artery Disease
About this trial
This is an interventional treatment trial for Coronary Artery Disease focused on measuring coronary artery disease, coronary artery bypass grafting
Eligibility Criteria
Inclusion Criteria: Age more than 18 years old First time undergo isolated CABG surgery Severe three-vessel disease (Left anterior decending artery, Left circumflex artery, Right coronoary artery lesion with more than 75% stenosis) Exclusion Criteria: Urgent or Redo CABG surgery Concomitant cardiac or vascular procedures (i.e. valve repair or replacement, Morrow procedure) A positive Allen test, radial artery plaque on ultrasound or a history of vasculitis or Raynaud's syndrome Varicose great saphenous vein or venous tortuosity and judged as can not be used in operation by surgeons Known allergy to radiographic contrast media Planed endarterectomy of coronary artery before surgery Malignant tumor or other severe systemic diseases Combined with other irreversible organ failures Contraindications for dual antiplatelet therapy, such as active gastroduodenal ulcer Participant of other ongoing clinical trials in 30 days.
Sites / Locations
- Fuwai Hospital Chinese Academay of Medical Science and National Center for Cardiovascular Diseases
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
No-Touch vein
Radial artery
No-touch vein group has two No-touch saphenous vein grafts, anastomose to the right coronary or left coronary system. All patients also acquired LITA-LAD anastomosis to complete the revascularization.
Radial artery group has one radial artery graft and one conventional saphenous vein graft, anastomose to the right coronary or left coronary system basing on surgeons' decision. All patients also acquired LITA-LAD anastomosis to complete the revascularization.