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Study identifier: NCT06858020 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

NoPro - Norwegian Hernia Prophylaxis Study

Condition: Incisional Hernia After Midline Laparotomy · Quality of Life (QOL) · Burst Abdomen  ·  Sponsor: Sykehuset Innlandet HF

PhaseNA
Planned participants150
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Gjertrud H Kjostolfsen, MD  ·  0047 90236405  ·  gjertrud.hole.kjostolfsen@sykehuset-innlandet.no

Jorunn Skattum, MD PhD  ·  0047 90236680  ·  jorunn.skattum@sykehuset-innlandet.no

Always discuss trial participation with your own doctor first.

Locations (1)

Innlandet Hospital TrustHamar, NorwayRecruiting

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Source record: clinicaltrials.gov/study/NCT06858020