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Antimicrobial Hernia Repair Device Clinical Study — AMEX  

Ventral Hernia Clinical Trial

Official title:
Feasibility Study of the Antimicrobial Hernia Repair Device for Repair of Ventral or Incisional Hernia

Clinical Trial Summary

This prospective clinical study will evaluate the safety and efficacy of the Cook® Antimicrobial Hernia Repair Device containing an antimicrobial to reinforce soft tissue during ventral or incisional hernia repair in clean-contaminated, contaminated, and dirty-infected (i.e., Class II, Class III, and Class IV) surgical fields. Up to 30 patients will be treated with the Cook® Antimicrobial Hernia Repair Device and patients will be followed for 12 months.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02401334
Study type Interventional
Source Cook Group Incorporated
Contact
Status Completed
Phase N/A
Start date June 2015
Completion date January 25, 2018
View Details
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