Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Intra-abdominal Pressure During Hernia Repair

Official title: Assessment of Intra-abdominal Pressure During the Perioperative Period of Hernia Repair

Run by Centre Hospitalier Universitaire de Nice · NCT07531615 · Data updated 2026-11-12

This study tests perioperative abdominal pressure during open midline incisional hernia repair to see how pressure relates to outcomes in adults with moderate to large defects.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment10 (estimated)
SponsorCentre Hospitalier Universitaire de Nice
Academic / other
Locations1 site (Nice, Alpes-Maritimes)
StatusRecruiting
StartedJuly 30, 2026
Main results expectedMarch 1, 2028
Study endsAugust 1, 2028
Registry record updatedJuly 2, 2026
Trial IDNCT07531615 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with midline incisional hernias having 4–10 cm transverse defect width and EHS M2–M4 locations, undergoing elective open repair with retromuscular mesh at CHU de Nice.

Probably not a fit

Patients undergoing different surgical approaches, smaller or larger defects, or those not meeting inclusion criteria may not experience a benefit from these findings.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The trial examines intra-abdominal pressure measurements taken during open midline incisional hernia repairs with retromuscular mesh placement. It is an interventional, non-randomized study conducted at CHU de Nice, focusing on patients with specific defect sizes (4–10 cm) and EHS M2–M4 locations. The goal is to understand how perioperative pressure may influence recurrence risk and inform surgical technique choices. Exclusion criteria include alternative hernia types, laparoscopic approaches, pregnancy, and certain legal protections. Results could help refine techniques to reduce recurrence and complications after repair.

Why it matters

Potential benefit: If successful, the findings could guide surgeons on optimal intra-abdominal pressure targets to minimize recurrence and improve recovery after open midline incisional hernia repair.

How similar studies have gone: Previous work has explored tension-free repairs and pressure dynamics, but direct perioperative intra-abdominal pressure testing in this specific repair context remains limited, making this approach relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Midline incisional hernias with a hernia defect width between 4 and 10 cm in the transverse axis, corresponding to W2 according to the EHS classification
* M2, M3, and M4 locations according to the EHS classification (i.e., hernia defects located from 3 cm below the xiphoid process to 3 cm above the upper border of the pubic symphysis)
* Patients scheduled for elective open midline incisional hernia repair with retromuscular mesh placement
* Provision of written informed consent
* Affiliation with a national health insurance system

Exclusion Criteria:

* Other types of incisional hernia
* Minimally invasive surgery (laparoscopic or robotic approach)
* Patients under legal protection (guardianship or curatorship), or patients unable to participate in a clinical study in accordance with Article L.1121-16 of the French Public Health Code
* Pregnant or breastfeeding women of childbearing age

Where it's running

  • CHU de Nice
    Nice, Alpes-Maritimes, France
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.