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Clinical Trials/NCT00235846
NCT00235846
Completed
Not Applicable

Endoscopic Vessel Harvesting During Coronary Bypass Surgery

Aalborg University Hospital1 site in 1 country132 target enrollmentDecember 2004

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Coronary Arteriosclerosis
Sponsor
Aalborg University Hospital
Enrollment
132
Locations
1
Primary Endpoint
Patient satisfaction
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

Conventional open vein harvesting from the legs during coronary artery bypass surgery result in wound complications among 30% of the patients. Endoscopic harvesting decrease the complication rate, but it remains to be shown whether this is also a fact among patient in whom only short segments of veingraft material is needed from the leg. We hypothesise that the rate of wound complications will be reduced and the patient satisfaction will be increased also among patients in whom only short vein segments are endoscopically harvested compared to conventional open vein harvesting.

Detailed Description

Conventional open vein harvesting from the legs during coronary artery bypass surgery result in wound complications among 30% of the patients. Endoscopic harvesting decrease the complication rate, but it remains to be shown whether this is also a fact among patient in whom only short segments of veingraft material is needed from the leg. We hypothesise that the rate of wound complications will be reduced and the patient satisfaction will be increased also among patients in whom only short vein segments are endoscopically harvested compared to conventional open vein harvesting. Preoperative demographic as well ass peri- and postoperative data are collected prospectively at 5-7 days and 1 month postoperatively. Wound complications are registered as well as post operative pain in the wound is evaluated using af visual analogue scale. Patients are evaluating the cosmetic results after wound healing.

Registry
clinicaltrials.gov
Start Date
December 2004
End Date
July 2007
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jan Jesper Andreasen, MD, PhD

Professor

Aalborg University Hospital

Eligibility Criteria

Inclusion Criteria

  • Elective coronary artery bypass surgery

Exclusion Criteria

  • Leg wounds
  • Acute surgery
  • Previous vascular surgery
  • Combined surgery (valve + coronary)
  • Arterial revascularization

Outcomes

Primary Outcomes

Patient satisfaction

Time Frame: 30 days

Rate of wound complications

Time Frame: 30 days

Study Sites (1)

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