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Clinical Trial Summary

The purpose of this study is to collect additional safety data and demonstrate the performance of Integra Gentrix® Surgical Matrix for reinforcement of ventral hernia repairs.


Clinical Trial Description

Retrospective data will be collected and assessed for early post-operative surgical site events and complications in the immediate post-operative period of 90 days. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05610267
Study type Observational
Source Integra LifeSciences Corporation
Contact
Status Completed
Phase
Start date November 22, 2022
Completion date December 28, 2022

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