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Study of Phasix™ Mesh for VHWG Grade 3 Midline Hernia Repair

Hernia Clinical Trial

Official title:
A Post-Market, Prospective, Multi-Center, Single-Arm Clinical Investigation of Phasix™ Mesh for VHWG Grade 3 Midline Hernia Repair

Clinical Trial Summary

The purpose of this study is to collect additional data on safety and performance of Phasix™ Mesh in subjects requiring Ventral Hernia Working Group (VHWG) Grade 3 midline hernia repair.

Clinical Trial Description

Approximately 85 subjects, at approximately 12 sites across Europe will be enrolled and treated to study the use of Phasix™ Mesh. All treated subjects will be followed for 2 years post-implantation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02720042
Study type Interventional
Source C. R. Bard
Contact
Status Completed
Phase N/A
Start date March 23, 2016
Completion date June 20, 2019
View Details
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