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Clinical Trial Summary

The study aim is to assess polyethylene glycol (PEG) coated collagen patch (Hemopatch) on the quality of drainage after surgery, the length of hospital stay, the number of reoperations due to haemorrhage and treatment cost. The study will be conducted in 200 patients undergoing Coronary Artery Bypass Grafting (CABG) with the use of extracorporeal circulation and Internal mammary Artery (IMA) harvesting. Traditional method of haemostasis will be applied in 100 patients and Hemopatch will be additionally used in 100 subjects to prevent haemorrhage after IMA harvesting and sternum closure.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03340090
Study type Interventional
Source Medical Universtity of Lodz
Contact Michal Krejca, PhD,Md
Phone +48422014460
Email michal.krejca@umed.lodz.pl
Status Recruiting
Phase N/A
Start date March 20, 2018
Completion date December 31, 2019

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