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Post Market Study of Parietene™ DS Composite Mesh in Ventral Hernia Repair — PPDS  

Ventral Hernia Clinical Trial

Official title:
A Multi-center Post-market Single Arm Prospective Study of Parietene™ DS Composite Mesh in Subjects Undergoing Ventral Hernia Repair

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

Clinical Trial Details
NCT number NCT03495154
Study type Interventional
Source Medtronic - MITG
Contact
Status Completed
Phase N/A
Start date June 21, 2018
Completion date July 6, 2022
View Details
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