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Comparative Study of Biologic Mesh Versus Repair With Component Separation. — Davol  

Ventral Hernia Clinical Trial

Official title:
Randomized Control Trial of Biologic Mesh (XenMATRIXTM) vs. Component Separation Alone in Contaminated Ventral Hernia Repair:a Pilot Study

Clinical Trial Summary

The purpose of this study is to compare open abdominal incisional hernia repair using XenMATRIX biologic mesh versus repair with their own tissue. This study will provide information in determining if a biological mesh is necessary to provide a sturdy repair for a ventral hernia.

Clinical Trial Description

This study will involve comparison of open abdominal incisional hernia repair with XenMATRIX biologic graft versus repair with native tissue. The current study seeks to evaluate XenMATRIXTM, an FDA approved biologic graft for repairing contaminated abdominal wall defects. This study will provide significant insight for the reconstructive surgeon and patient to determine whether a biologic graft is necessary for the reconstruction of a contaminated ventral hernia repair to provide a durable single staged repair. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01295125
Study type Interventional
Source University Hospitals Cleveland Medical Center
Contact
Status Terminated
Phase N/A
Start date January 2011
Completion date May 2012
View Details
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