NoPro - Norwegian Hernia Prophylaxis Study
Recruiting
N/A
Interventional Study
Incisional Hernia After Midline Laparotomy
Quality of Life (QOL)
Burst Abdomen
Surgical Site Infections
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 150 (estimated)
- Sponsor
- Sykehuset Innlandet HF · Other
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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.
Trial Locations
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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 re…
Contacts