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Recruiting NCT06858020

NoPro - Norwegian Hernia Prophylaxis Study

Trial Parameters

Condition Incisional Hernia After Midline Laparotomy
Sponsor Sykehuset Innlandet HF
Study Type INTERVENTIONAL
Phase N/A
Enrollment 150
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-02-17
Completion 2028-12
Interventions
Prophylactic polypropylene onlay mesh

Brief Summary

A multicenter randomized controlled trial comparing midline laparotomy closures using the small-bite suture technique alone to those using the small-bite suture technique with an additional onlay prophylactic polypropylene mesh. The primary endpoint is the incidence of incisional hernias in both groups after one year.

Eligibility Criteria

Inclusion Criteria: * Surgery predominantly done my midline laparotomy * Age 18 years old or older * Written consent by patient/family * Midline laparotomy with delayed closure * No exclusion criteria Exclusion Criteria: * Age under 18 years * Pregnancy * Previous abdominal midline hernia mesh repair * Abdominal compartment syndrome * Linea alba closure not possible * Life expectancy under six months * Hernia in the midline with transverse diameter lager than 2 cm

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