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Clinical Trial Summary

This trial is being conducted to evaluate the efficacy of Phasix™ Mesh implantation at the time of midline fascial closure compared to primary suture closure in preventing a subsequent incisional hernia in subjects at risk for incisional hernia after open midline laparotomy surgery.


Clinical Trial Description

Subjects will be randomized (1:1) to one of the two treatment groups in the operating room after fascial closure. ;


Study Design


NCT number NCT03911700
Study type Interventional
Source C. R. Bard
Contact Amanda Resendes, MBA
Phone 401-209-7141
Email amanda.resendes@bd.com
Status Recruiting
Phase N/A
Start date December 12, 2019
Completion date September 2031