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Prospective Randomised comparison of Off-pump and on-pump MultIvessel coronary artery bypasS Surgery: analysis of early graft patency by multi-slice computed tomography

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN58800729
Enrollment
150
Registered
2008-03-19
Start date
2005-04-19
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multivessel coronary artery disease Circulatory System Cronary artery disease

Interventions

Patients undergo coronary artery bypass grafting with internal mammary artery, radial or saphenous vein in the two groups using the same anaesthetic protocol, the same graft anastomotic techniques and

Sponsors

Hospital da Cruz Vermelha (Portugal)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients between 30 and 90 years 2. Multivessel disease 3. Indication for primary coronary artery bypass graft (CABG) for at least three distal anastomoses according to consensus given by two independent surgeons

Exclusion criteria

Exclusion criteria: 1. Patient requiring emergency surgery such as: 1.1. Ventilatory support 1.2. Intravenous inotropic therapy 1.3. Cardiogenic shock 1.4. Catheterism accident 1.5. Q-wave myocardial infarction in evolution 2. Need for associated procedures 3. Renal insufficiency or serum creatinine 1.5 times superior to the upper limit normal values 4. Atrial fibrillation 5. Known allergy to contrast material 6. Dyspnoea at rest or inability to hold breath 7. Women with child bearing potential (for the purpose of this study women which have menopause for less than 12 months will be excluded, with exception for those with surgical menopause) 8. Inability to give inform consent

Design outcomes

Primary

MeasureTime frame
Graft patency at 4 - 6 weeks evaluated by 16 slice computed tomography.

Secondary

MeasureTime frame
1. Post-operative adverse events 2. Neurocognitive testing at baseline and 4 - 6 weeks 3. Quality of life at baseline and 6 months 4. Adverse events and stress test at 6 months

Countries

Portugal

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 5, 2026