Phase 1 Completed NCT01488084

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

Sunnybrook Health Sciences Centre · Interventional, Randomized

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Completed November 2012. Read the results summary below →
Study context Single-site study

Overview

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.

Full record on ClinicalTrials.gov (NCT ID NCT01488084).

Results summary

None

Outcome data

EndpointTypeResultSignificance
Biological Properties Primary None None
Leg wound Healing and Leg Functional Outcome Secondary None None

Full results record on ClinicalTrials.gov.

Study design

Phase
Phase 1
Study type
Interventional
Allocation
Randomized
Masking
Double-blind
Intervention model
Parallel assignment
Primary purpose
Treatment
Enrollment (final)
15 participants
Actually completed
November 2012

Recruitment criteria

Age range: 18–80 · Sex: All · Healthy volunteers: Requires diagnosis

Locationsi

1 site participated during the trial period. Representative sites shown below; full historical record on ClinicalTrials.gov.

Sunnybrook Health Sciences Centre — Toronto, Ontario (Canada)

Sources

REG
ClinicalTrials.gov — NCT01488084
Trial registry · primary record
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