MedPath

Five-year Patency of No-touch Saphenous Vein Grafts in On-pump Versus Clamp-less Off-pump Coronary Artery Bypass Surgery

Not Applicable
Completed
Conditions
Coronary Artery Stenoses
Registration Number
NCT03447197
Lead Sponsor
Örebro County Council
Brief Summary

Randomised controlled trials (RCTs) have shown high long-term patency for no-touch saphenous vein grafts (NTSVGs), comparable to the internal thoracic artery in on-pump coronary artery bypass grafting (CABG). RCTs on patency in NTSVGs in off-pump CABG have not been published yet. Orebro University Hospital participated in the CABG Off- or On-pump Revascularization study (CORONARY, ClinicalTrials.gov number, NCT00463294) and included fifty-six patients. Accordingly, this is a sub-study and the aim was to assess the midterm patency in NTSVGs in clamp-less off-pump versus on-pump CABG at five-year follow-up.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
59
Inclusion Criteria
  • Patients were eligible if they:

    1. provided written informed consent;

    2. were >21 years of age;

    3. required isolated CABG with median sternotomy;

    4. had at least one of the following risk factors:

      1. had peripheral vascular disease (previous peripheral bypass, amputation or anklebranchial index <0.90),
      2. had cerebrovascular disease (history of stroke, transient ischemic attach or carotid stenosis ≥70%),
      3. had renal insufficiency (creatinine above upper limit of normal),
      4. were ≥70 years of age, or
      5. were between the ages of 60-69 with one of the following: i. had diabetes and taking an oral hypoglycemic agent and/or insulin, ii. required urgent revascularization (i.e., waiting in hospital for revascularization after an acute coronary syndrome), iii. were a recent smoker (within 1 year of randomization), or iv. had left ventricular ejection fraction ≤35%, OR
      6. were between the ages of 55-59 with two of the following: i. Diabetes and taking an oral hypoglycemic agent and/or insulin, ii. required urgent revascularization (i.e., waiting in hospital for revascularization after an acute coronary syndrome, iii. were a recent smoker (within 1 year of randomization), or iv. had a left ventricular ejection fraction ≤35%
Exclusion Criteria
  • Patients were excluded if they:

    1. required a concomitant cardiac procedure associated with CABG;
    2. had a contraindication to off-pump or on-pump CABG (e.g., calcified aorta, intramuscular left anterior descending artery, calcified coronaries, small target vessels);
    3. had a concomitant life-threatening disease likely to limit life expectancy to less than 2 years;
    4. were previously enrollment in the CORONARY Trial;
    5. required emergency CABG surgery (i.e., immediate revascularization for hemodynamic instability); OR
    6. required a redo CABG.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Graft patencyFive years postoperatively

Graft patency as assessed with computed tomography angiography

Secondary Outcome Measures
NameTimeMethod

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.