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Completed

NCT Number: NCT01488084

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

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.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Sunnybrook Health Sciences Centre

Toronto, Ontario, M4N 3M5, Canada

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age> 18 years and able to provide informed consent
  • Requiring isolated, primary coronary artery bypass graft surgery
  • Elective or urgent cases
  • With or without the use or cardiopulmonary bypass
  • Left ventricular ejection fraction > 20%
  • Patient require at least 2 SVG's

Exclusion criteria

  • Unable to give consent
  • Unable to use bilateral lower greater saphenous veins ( severe peripheral vascular disease,varicose veins, previous vein stripping, previous amputation, inadequate ultrasound appearance )
  • Pregnant women, women of child bearing age
  • Preoperative persistent atrial fibrillation

Treatment and study plan

Coronary Artery Bypass Graft Surgery

Procedure

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

Conventional open SVG harvesting

Procedure

SVG harvested using conventional open technique and manually distended with crystalloid solution

Primary outcomes

  1. Biological Properties

    Time frame: 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 outcomes

  1. Leg wound Healing and Leg Functional Outcome

    Time frame: 12 months postoperatively

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

Sponsors and collaborators

Lead sponsor

Sunnybrook Health Sciences Centre

Other

Collaborators

  • Unity Health Toronto

Registry information

Official study title

Comparative Evaluation of Vasomotor Function in Saphenous Veins Harvested Using Pedicled vs Conventional Technique

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Dec 8, 2011
Registry last updated
Dec 12, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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