# Prophylactic Mesh Implantation in Patients With Peritonitis for the Prevention of Incisional Hernia

> **NCT01802164** · NA · TERMINATED · sponsor: **Insel Gruppe AG, University Hospital Bern** · enrollment: 5 (actual)

## Conditions studied

- Peritonitis
- Incisional Hernia
- Surgery

## Interventions

- **DEVICE:** A non-absorbable composite mesh (Ethicon Physiomesh)

## Key facts

- **NCT ID:** NCT01802164
- **Lead sponsor:** Insel Gruppe AG, University Hospital Bern
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2013-03
- **Primary completion:** 2015-04
- **Final completion:** 2015-04
- **Target enrollment:** 5 (ACTUAL)
- **Why stopped:** Recruitment problems due to very restricted inclusion criteria
- **Last updated:** 2015-06-16


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01802164

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01802164, "Prophylactic Mesh Implantation in Patients With Peritonitis for the Prevention of Incisional Hernia". Retrieved via AI Analytics 2026-06-01 from https://api.ai-analytics.org/clinical/NCT01802164. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
