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Post-Market Evaluation of HEMOBLAST™ Bellows in Laparoscopic Abdominal, Gynecological, and Urological Surgery — NOBLE-Laparo  

Hemostasis Clinical Trial

Official title:
Post-Market Evaluation of HEMOBLAST™ Bellows Performance and Safety in Laparoscopic Abdominal, Gynecological and Urological Surgery

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

Clinical Trial Details
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
View Details
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