Study of Endoscopic Versus Open Harvest of the Radial Artery in Coronary Artery Bypass Surgery

Sponsor
Lawson Health Research Institute (Other)
Overall Status
Completed
CT.gov ID
NCT00303706
Collaborator
Johnson & Johnson (Industry)
119
1
28
4.3

Study Details

Study Description

Brief Summary

The purpose of this study is to compare the safety and effectiveness of minimally invasive endoscopic harvest of the radial artery to the conventional open method of radial artery harvest in coronary artery bypass surgery. The researchers hypothesize that the radial artery can be safely, efficiently, and routinely harvested using a minimally invasive endoscopic technique. Endoscopic minimally invasive harvesting of the radial artery will reduce the postoperative morbidity due to pain, wound infection, and neurological complications and improve cosmetic results.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Endoscopic Radial Artery Harvest
Phase 2/Phase 3

Detailed Description

Many surgical disciplines have been quick to adopt minimally invasive techniques because of decreased complications and shorter recovery times. As we enter the fifth decade of coronary artery bypass grafting surgery more attempts are being made to perform the operation less invasively. Harvesting of the saphenous vein (a large superficial vein in the leg which is routinely used in bypass surgery) using a telescope (camera), has been shown to be superior to harvesting the vein through a large open incision. At our institution, this vein mentioned above, is routinely harvested using less invasive techniques with a camera. This has been shown to result in less infection.

In the early 1990's, the radial artery was reintroduced into bypass surgery to increase the number of available alternative bypass grafts. Long-term results of the radial artery (8-9 years) have shown that 88-91% of the radial arteries harvested remain open thereby allowing the flow of blood. This is significantly better than the 10-year rates of the saphenous vein of 53-67%. Therefore, the radial artery has become more popular as a bypass graft.

Conventionally, the radial artery is harvested by making a long vertical incision extending from the wrist to the elbow. The radial artery is then dissected under direct vision within this large open incision. Complications from the open harvest of the radial artery include infection, neurological complications, possible decrease blood flow to the hand, and poor wound healing or scarring.

Recently, with the development of endoscopic harvesting systems, the radial artery can be harvested using a telescope (camera) and very small incisions. Thus far, to our knowledge there have been no published studies comparing conventional techniques to less invasive endoscopic techniques for harvesting the radial artery. Therefore, we propose a prospective randomized study to determine if the radial artery can be routinely harvested using an endoscopic minimally invasive technique. We wish to compare the conventional open technique to the minimally invasive technique to determine if there are any differences in postoperative complications, length of hospital stay or possible differences in patient satisfaction in cosmetic results (scarring) between the two techniques.

Study Design

Study Type:
Interventional
Actual Enrollment :
119 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Prospective Randomized Trial of Endoscopic Versus Conventional Harvesting of the Radial Artery in Coronary Artery Bypass
Actual Study Start Date :
Apr 1, 2005
Actual Study Completion Date :
Aug 1, 2007

Outcome Measures

Primary Outcome Measures

  1. The primary outcome event will be the rate of forearm wound infection at 6 weeks. [6 weeks]

Secondary Outcome Measures

  1. Wound pain [6 weeks]

  2. Neurological complications [6 weeks]

  3. Patient satisfaction [6 weeks]

  4. Length of hospitalization [will vary with patient lenght of stay]

  5. Histological integrity of the harvested radial artery [during OR]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Eligible patients greater than 18 years of age with coronary artery disease requiring elective, urgent, or emergency coronary artery revascularization where the radial artery can be used as a bypass conduit.
Exclusion Criteria:
  • Patient's refusal to have surgery, inability to give informed consent, and contraindication in harvesting the radial artery.

Contacts and Locations

Locations

Site City State Country Postal Code
1 London Health Sciences Centre, University Hospital London Ontario Canada N6A 5A5

Sponsors and Collaborators

  • Lawson Health Research Institute
  • Johnson & Johnson

Investigators

  • Principal Investigator: Bob Kiaii, MD, FRCSC, Department of Cardiac Surgery, University of Western Ontario and the London Health Sciences Centre, University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00303706
Other Study ID Numbers:
  • R-05-053
First Posted:
Mar 17, 2006
Last Update Posted:
Feb 17, 2020
Last Verified:
Feb 1, 2020

Study Results

No Results Posted as of Feb 17, 2020