Clinical Trial

Comparing PP and PVDF Meshes in Midline Laparotomy Closure for High-risk Colorectal Surgery. Impact on Incisional Hernia and Surgical Wound Infection.

Study acronym: PROFIMESH
Recruiting
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Record status
This record was last updated October 8, 2024 (before its estimated January 15, 2025 completion). Its status may not reflect the trial's current state.
Summary
In the latest guidelines for abdominal wall closure in emergency surgery published in the World Journal of Emergency Surgery (WJES) in 2023, no specific recommendations are made in this regard. Current literature does not provide any articles comparing these two types of mesh materials (PP vs PVDF) in emergency colorectal surgery. It is necessary to conduct a study comparing these two types of mesh materials, specifically in high-risk patients for incisional hernia and emergency colorectal surgery. This study aims to contribute to generating evidence regarding differences in wound infection incidence and potential subsequent complications, such as chronic pain. It is essential to conduct a study comparing different methods of laparotomy closure, specifically in emergency colorectal surgery, to contribute valuable evidence regarding the incidence of incisional hernia and potential subsequent complications.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-01-22.
Trial Details
NCT Number NCT06220045
Lead Sponsor Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta
Conditions Colorectal Cancer, Wound Infection, Hernia Incisional
Enrollment 60 participants
Start Date 2024-02-01
Primary Completion 2025-01-15 (estimated)
Study Completion 2025-01-15 (estimated)
Updated on ClinicalTrials.gov 2024-10-08