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PROPHYlactic Implantation of BIOlogic Mesh in Peritonitis (PROPHYBIOM) — PROPHYBIOM  

Incisional Hernia Clinical Trial

Clinical Trial Summary

To evaluate the efficacy of the use of swine dermal collagen prosthesis implanted preperitoneally as a prophylactic procedure against incisional hernia in patients operated in urgency/emergency setting in contaminated/infected fields with peritonitis. The aim of the study is to reduce the incidence of incisional hernia from 50% to 20%.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02277262
Study type Interventional
Source A.O. Ospedale Papa Giovanni XXIII
Contact
Status Recruiting
Phase Phase 4
Start date October 2014
Completion date October 2018
View Details
See also
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