Assessing Vein Graft Properties Between Conventional & No-Touch Harvesting Technique - (PATENT SVG)

Sponsor
Sunnybrook Health Sciences Centre (Other)
Overall Status
Completed
CT.gov ID
NCT01488084
Collaborator
Unity Health Toronto (Other)
15
1
2
29
0.5

Study Details

Study Description

Brief Summary

The purpose of this study is to compare saphenous veins harvested using the atraumatic pedicled ("no-touch") technique to saphenous veins harvested using the conventional open technique in patients undergoing isolated coronary artery bypass surgery. Investigators will compare the biological structure of the saphenous veins harvested using these two techniques. There is some evidence that saphenous veins harvested using the "no-touch" technique may allow for better patency up to 8 years following bypass surgery. We may be able to detect early differences in vascular structure, observed at the time of conduit harvest.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Coronary Artery Bypass Graft Surgery
  • Procedure: Conventional open SVG harvesting
Phase 1

Detailed Description

Atherosclerosis is a complex, multifactorial inflammatory disease, which is initiated largely in areas of endothelial injury, secondary to biomechanical disturbances, or systemic factors such as lipoprotein disturbances, hypertension, diabetes, and smoking (the response to injury hypothesis). Accumulating data indicate that structural and/or functional alterations in endothelial integrity play a primordial role in the development of atherosclerosis via promoting aberrant interactions between modified lipoproteins, monocyte-derived macrophages, T cells and normal cellular elements of the arterial wall inciting early plaque formation. As such, strategies, either pharmacological or mechanical in nature which reduce and/or restore endothelial homeostasis remain an important cornerstone to limit atherosclerosis.

Investigators hypothesize that saphenous veins harvested using the atraumatic pedicled ("no-touch") technique from patients undergoing isolated coronary artery bypass surgery will exhibit superior indices of vasomotor structure compared to veins harvested using the conventional open technique. We anticipate that leg healing will not be significantly altered using the "no-touch" technique.

Eligible patients will have two SVG segments harvested, one from each lower leg. One leg will have the SVG harvested in the conventional fashion and the contralateral leg will have the SVG harvested using the "no touch" technique. This will be determined by block randomization revealed at the time of skin incision. For patients with very small lower leg saphenous veins, the surgical protocol would be to then use the thigh segment instead. Patients will have Duplex scans to evaluate saphenous veins pre-operatively.

Study Design

Study Type:
Interventional
Actual Enrollment :
15 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Comparative Evaluation of Vasomotor Function in Saphenous Veins Harvested Using Pedicled vs Conventional Technique
Study Start Date :
Jun 1, 2010
Actual Primary Completion Date :
Aug 1, 2012
Actual Study Completion Date :
Nov 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: Pedicled "no-touch" SVG harvesting

Saphenous vein harvested with a pedicle of surrounding fat and distension with heparinized blood at arterial pressure. No manual distention.

Procedure: Coronary Artery Bypass Graft Surgery
Comparison of two techniques of saphenous vein graft harvesting for coronary artery bypass graft surgery
Other Names:
  • Pedicled "no-touch" saphenous vein graft harvesting
  • Conventional open saphenous vein graft harvesting
  • Active Comparator: Conventional open SVG harvesting

    Saphenous vein is harvested with an open technique, stripped of adventitia, and manually distended with crystalloid solution.

    Procedure: Coronary Artery Bypass Graft Surgery
    Comparison of two techniques of saphenous vein graft harvesting for coronary artery bypass graft surgery
    Other Names:
  • Pedicled "no-touch" saphenous vein graft harvesting
  • Conventional open saphenous vein graft harvesting
  • Procedure: Conventional open SVG harvesting
    SVG harvested using conventional open technique and manually distended with crystalloid solution

    Outcome Measures

    Primary Outcome Measures

    1. Biological Properties [Characteristics of the tissue will be reflective of the status of the tissue on the day of surgery (day 0).]

      Segments of saphenous veins, approximately 5cm in length, harvested by either the conventional or no-touch technique will be employed. Segments will be immediately frozen in liquid nitrogen for Western blot analysis. Another 5mm segment will be used for immediate measurement of superoxide (O2-) production. Two rings, approximately 5mm in length will be frozen in Tissue Teck and another one placed in formalin (4%) and then embedded in paraffin.

    Secondary Outcome Measures

    1. Leg wound Healing and Leg Functional Outcome [12 months postoperatively]

      Leg wound healing and functional outcome will be assessed in both lower legs using a quality of life measurement tool.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Age> 18 years and able to provide informed consent

    2. Requiring isolated, primary coronary artery bypass graft surgery

    3. Elective or urgent cases

    4. With or without the use or cardiopulmonary bypass

    5. Left ventricular ejection fraction > 20%

    6. Patient require at least 2 SVG's

    Exclusion Criteria:
    1. Unable to give consent

    2. Unable to use bilateral lower greater saphenous veins ( severe peripheral vascular disease,varicose veins, previous vein stripping, previous amputation, inadequate ultrasound appearance )

    3. Pregnant women, women of child bearing age

    4. Preoperative persistent atrial fibrillation

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Sunnybrook Health Sciences Centre Toronto Ontario Canada M4N 3M5

    Sponsors and Collaborators

    • Sunnybrook Health Sciences Centre
    • Unity Health Toronto

    Investigators

    • Principal Investigator: Stephen Fremes, MD, Sunnybrook Health Sciences Centre

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Stephen E. Fremes, Head, Division of Cardiac and Vascular Surgery, Sunnybrook Health Sciences Centre
    ClinicalTrials.gov Identifier:
    NCT01488084
    Other Study ID Numbers:
    • 078-2009
    First Posted:
    Dec 8, 2011
    Last Update Posted:
    Dec 12, 2012
    Last Verified:
    Dec 1, 2012
    Keywords provided by Stephen E. Fremes, Head, Division of Cardiac and Vascular Surgery, Sunnybrook Health Sciences Centre
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 12, 2012