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GORE® ENFORM Biomaterial Product Study — ENF 18-06  

Incisional Hernia Clinical Trial

Official title:
GORE® ENFORM Biomaterial Product Study: A Study to Describe Multi-use Biomaterial Performance in Hernia Patients

Clinical Trial Summary

A prospective, retrospective, non-randomized, multicenter study with two independent hernia study cohorts (Ventral / Incisional Hernia Repair and Diaphragmatic / Hiatal Hernia Repair). The primary objective of this study is to collect GORE® ENFORM Biomaterial product commercial-use data on device functional performance.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04718168
Study type Interventional
Source W.L.Gore & Associates
Contact Bronte Emery
Phone 800-437-8181
Email ENF1806@wlgore.com
Status Recruiting
Phase N/A
Start date May 17, 2021
Completion date April 2025
View Details
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