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Prevention of Incisional Hernia With Biosynthetic Mesh at the Site of Temporary Ileostomy Closure (PRINCESS) — PRINCESS  

Incisional Hernia Clinical Trial

Official title:
Prevention of Incisional Hernia With Biosynthetic Mesh at the Site of Temporary Ileostomy Closure

Clinical Trial Summary

Prophylactic mesh reinforcement of the abdominal wall at the site of temporary ileostomy closure is effective in preventing postoperative incisional hernia. This prospective, multicenter, observational study will evaluate performance of Phasix biosynthetic mesh when used to reinforce fascial closure .

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05400083
Study type Observational [Patient Registry]
Source Federico II University
Contact Umberto Bracale, Prof
Phone +390817462544
Email umbertobracale@gmail.com
Status Recruiting
Phase
Start date May 17, 2021
Completion date May 2024
View Details
See also
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