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Clinical Trial Summary

A prospective, multi-center, multi-national single arm study to evaluate the performance and safety of HEMOBLAST™ Bellows in laparoscopic abdominal, gynecological, and urological surgery.


Clinical Trial Description

A prospective, multi-center, multi-national single arm study conducted in Austria, France, and Germany to evaluate the performance and safety of HEMOBLAST™ Bellows in laparoscopic abdominal, gynecological, and urological surgery. Up to 100 subjects will be enrolled at up to 10 sites, with a minimum of 8 subjects enrolled in each surgical specialty. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03873181
Study type Observational
Source Biom'Up France SAS
Contact
Status Completed
Phase
Start date May 16, 2019
Completion date August 26, 2020

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