Coronary Artery Bypass Grafting Strategies for the Anterolateral Territory: a Prospective Randomized Clinical Trial
Launched by CENTRE HOSPITALIER DE L'UNIVERSITÉ DE MONTRÉAL (CHUM) · Apr 24, 2012
Trial Information
Current as of August 02, 2025
Completed
Keywords
ClinConnect Summary
Purpose: This novel surgical design use a composite-sequential venous graft to distribute left anterior mammary artery (LIMA) inflow directly to the left anterior descending coronary (LAD), but also to the other branches of the anterolateral territory thereby promoting a higher flow through the LIMA pedicle. It is constructed using a short saphenous vein graft (SVG) bridge (LSVB) interposed between the LAD and one (or more) other anterolateral targets, with the LIMA grafted on the hood of the SVG just above the LAD anastomosis.
Objectives. The main objective of the prospective randomized c...
Gender
ALL
Eligibility criteria
- Inclusion Criteria: Patients who undergo coronary artery bypass grafting (CABG) surgery (for single, double or triple vessel disease) will be eligible if they:
- • 1. require isolated CABG with median sternotomy on at least one left anterior descending (LAD) site and another anterolateral target;
- • 2. provide written informed consent;
- • 3. are more than 21 years of age.
- Exclusion Criteria: A patient will be excluded from the study if he/she does not fulfill the inclusion criteria, the patient or the treating physician refuse the study or if any of the following are observed:
- • 1. concomitant cardiac procedure associated with CABG including valve surgery and ascending aorta surgery;
- • 2. contra-indications to cardiopulmonary bypass (calcified aorta);
- • 3. unusable left internal mammary artery (LIMA) such as uncorrected subclavian artery stenosis, anterior chest trauma, radiation or injury during harvesting precluding the use of the LIMA;
- • 4. concomitant life-threatening disease likely to limit life expectancy to less than 2 years;
- • 5. emergency CABG surgery (immediate revascularization for hemodynamic instability precluding patient consent);
- • 6. prior CABG;
- • 7. severe congestive heart failure with left ventricular ejection fraction less than 30%.
- Other exclusion criteria precluding MSCT include:
- • 8. moderate to severe renal impairment (estimated glomerular filtration rate, eGFR \<50 mL/min/1.73 m2);
- • 9. chronic atrial fibrillation (which can preclude ECG-gating during MSCT);
- • 10. history of severe hypersensitivity to iodinated contrast agents;
- • 11. known or suspected for pheochromocytoma;
- • 12. pregnant/lactating female.
- Furthermore, patients may be excluded at the time of MSCT if they are:
- • 13. in persistent rapid (\>100/min) atrial fibrillation or any other cardiac rhythm that precludes reliable ECG triggering;
- • 14. severe congestive heart failure, New York Heart Association (NYHA) Class IV, despite coronary revascularization and maximal medical treatment.
About Centre Hospitalier De L'université De Montréal (Chum)
The Centre Hospitalier de l'Université de Montréal (CHUM) is a leading academic health institution in Canada, dedicated to advancing patient care through innovative research and clinical excellence. As a prominent sponsor of clinical trials, CHUM is committed to leveraging its multidisciplinary expertise and state-of-the-art facilities to facilitate groundbreaking studies that enhance medical knowledge and improve health outcomes. Collaborating with a network of healthcare professionals and researchers, CHUM fosters a rigorous research environment that prioritizes patient safety, ethical standards, and scientific integrity, positioning itself at the forefront of medical advancements.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Montreal, Quebec, Canada
Patients applied
Trial Officials
Louis-Mathieu Stevens, MD, PhD (c)
Principal Investigator
Centre Hospitalier de l'Universite de Montreal (CHUM)
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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