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Ventral or Inguinal Hernia, Robotically Repaired With OviTex Mesh — BRAVOII  

Hernia, Inguinal Clinical Trial

Official title:
A Prospective Study Evaluating the Clinical Outcomes of Ventral or Inguinal Hernias Treated Robotically With OviTex® Reinforced Tissue Matrix

Clinical Trial Summary

This study is designed to evaluate the post-operative complications and hernia recurrence following the use of OviTex in subjects with ventral or inguinal hernias. Up to 160 subjects will participate in the study from up to 20 investigator sites.

Clinical Trial Description

This study is intended to evaluate the post-operative complications and recurrence following the use of OviTex in ventral or inguinal hernias being treated robotically. It is a single-arm study and all subjects will receive OviTex. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04779918
Study type Interventional
Source Tela Bio Inc
Contact Zachary Sterner
Phone 937-514-2262
Email zsterner@telabio.com
Status Recruiting
Phase N/A
Start date April 14, 2021
Completion date June 30, 2027
View Details
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