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Clinical Trial Summary

A prospective randomized, double-blinded, comparative within-person study to evaluate the use of SOMVC001 vs. heparin dosed saline in patients undergoing CABG.


Clinical Trial Description

Saphenous vein (SV) harvesting will be performed using an open or endoscopic vein harvesting technique. Once harvested, the SV will be divided into segments and these vein segments from each patient to be immersed in one of two blinded solutions: SOMVC001 or heparin dosed saline. The patients will then be randomized and SVG segment allocations will be defined and grafted to the assigned target regions. Imaging, using 64-slice or better MDCT, will be completed 4-6 weeks and 3 months post surgery (CABG) procedure. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02272582
Study type Interventional
Source Montreal Heart Institute
Contact
Status Completed
Phase N/A
Start date September 24, 2014
Completion date December 22, 2016

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