Prophylactic Reinforcement of Ventral Abdominal Incisions Trial

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.

NCT Number	NCT03911700
Lead Sponsor	C. R. Bard
Conditions	Open Midline Laparotomy
Enrollment	477 participants
Start Date	2019-12-12
Primary Completion	2029-12 (estimated)
Study Completion	2031-12 (estimated)
Updated on ClinicalTrials.gov	2026-06-12