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Clinical Trial Summary

The purpose of this prospective, randomized, controlled study is to evaluate the safety and efficacy of a new hemostatic device (HEMOBLAST™ Bellows) compared to a control device, absorbable gelatin sponge USP with thrombin.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02780869
Study type Interventional
Source Biom'Up SA
Contact
Status Completed
Phase N/A
Start date July 18, 2016
Completion date March 27, 2017

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