NoPro - Norwegian Hernia Prophylaxis Study

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorSykehuset Innlandet HF

About this trial

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

Qualifiers

Surgery predominantly done my midline laparotomy

Age 18 years old or older

Written consent by patient/family

Midline laparotomy with delayed closure

Disqualifiers

Age under 18 years

Pregnancy

Previous abdominal midline hernia mesh repair

Abdominal compartment syndrome

Trial design

Treatments tested in this trial

  • Prophylactic polypropylene onlay mesh

Treatment groups

150 Participants
are divided into 2 treatment groups

Sponsors and collaborators