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.
Description
Subjects will be randomized (1:1) to one of the two treatment groups in the operating room after fascial closure.
Principal Investigator
Bryan Richmond
Study Coordinator
Kristi Sutphin
Research Contact
CAMC Clinical Trials Center - 304.388.9944
Departments
Sex
All
Age
18+
NCT Number
NCT03911700
IRB Number
19-609