NoPro - Norwegian Hernia Prophylaxis Study

Last updated: February 28, 2025
Sponsor: Sykehuset Innlandet HF
Overall Status: Active - Recruiting

Phase

N/A

Condition

Hernia

Treatment

Prophylactic polypropylene onlay mesh

Clinical Study ID

NCT06858020
761933
  • Ages > 18
  • All Genders

Study 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

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

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

Study Design

Total Participants: 150
Treatment Group(s): 1
Primary Treatment: Prophylactic polypropylene onlay mesh
Phase:
Study Start date:
February 17, 2025
Estimated Completion Date:
December 31, 2028

Study Description

An incisional hernia (IH) is a defect in the abdominal wall at the site of a surgical scar, leading to the protrusion of abdominal contents through the defect. It is a common complication following midline laparotomy, with incidence rates ranging from 9% to 40% in the general population, and up to 69% in high-risk patients. Several studies have been conducted on the prevention of IH, and one established intervention is the use of a synthetic mesh to reinforce the suture closure of the abdomen after midline laparotomy. However, the use of mesh in this context is not widespread in Norway, and there are no Norwegian studies on IH prevention following midline laparotomy. This study aims to contribute to the broader knowledge base and encourage Norwegian surgeons to consider using prophylactic meshes.

The study will involve three Norwegian hospitals: Hamar Hospital, Gjøvik Hospital, and Lillehammer Hospital. Participants will be patients scheduled for midline laparotomy at these hospitals who consent to participate, meet the inclusion criteria, and do not meet any exclusion criteria. Participants will be randomly assigned to two groups, each receiving a different variation of fascia closure during laparotomy. One group will undergo closure using the standard small-bites technique only, while the other group will undergo closure with the small-bites technique in addition to an onlay polypropylene mesh.

The primary outcome is the occurrence of incisional hernia one year after surgery, identified through clinical examination and CT scan. Additionally, surgical site occurrences (e.g., hematoma, infection, seroma, wound dehiscence) will be recorded four to six weeks post-surgery. Quality of life and pain levels will also be assessed at both four to six weeks and one year after surgery.

Connect with a study center

  • Innlandet Hospital Trust

    Hamar,
    Norway

    Active - Recruiting

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