Negative Pressure Dressing After Saphenous Vein Harvest

Status Completed

Clinical Trial Summary

This study will test the effectiveness of negative pressure wound therapy (using the VAC Prevena device, KCI Canada Inc.) applied to the saphenous vein harvest site after Coronary Artery Bypass Grafting (CABG). When initiated immediately after surgery, this intervention may decrease the incidence of wound infection and non-infectious wound complications. It may decrease wound discomfort and improve mobility and functional recovery of the leg.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Complication of Coronary Artery Bypass Graft
Coronary Artery Disease
Coronary Disease
Myocardial Ischemia
Wound Complication

Clinical Trial Details

NCT number	NCT01698372
Study type	Interventional
Source	University of Calgary
Contact
Status	Completed
Phase	Phase 1
Start date	September 2012
Completion date	March 2015

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