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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


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

See also
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