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Clinical Trial Summary

A multi-center post-market single arm prospective study of Parietene™ DS Composite Mesh in subjects undergoing ventral hernia repair to confirm its clinical safety and performance in the short (1, 3 months), mid (12 months) and long term (24 months)


Clinical Trial Description

A multi-center post-market single arm prospective study of Parietene™ DS Composite Mesh in subjects undergoing ventral hernia repair to confirm its clinical safety and performance in the short (1, 3 months), mid (12 months) and long term (24 months)

125 male or female adults subjects will be enrolled in a minimum of 4 USA sites who are undergoing elective ventral hernia repair (primary or incisional) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03495154
Study type Interventional
Source Medtronic - MITG
Contact Michael PACE
Phone (781) 460-1554
Email michael.pace@medtronic.com
Status Recruiting
Phase N/A
Start date June 21, 2018
Completion date July 1, 2021

See also
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