# Reducing the Incidence of Incisional Hernia After Stoma Closure Using a Prophylactic Mesh

> **NCT04510558** · NA · UNKNOWN · sponsor: **University Hospital, Geneva** · enrollment: 72 (estimated)

## Conditions studied

- Incisional Hernia

## Interventions

- **DEVICE:** Stoma closure with non-resorbable mesh (ULTRAPRO Advanced Mesh, Ethicon, Johnson & Johnson) in the sublay position
- **PROCEDURE:** Stoma closure without mesh

## Key facts

- **NCT ID:** NCT04510558
- **Lead sponsor:** University Hospital, Geneva
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2021-05-01
- **Primary completion:** 2024-05
- **Final completion:** 2024-12
- **Target enrollment:** 72 (ESTIMATED)
- **Last updated:** 2023-09-13


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04510558

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04510558, "Reducing the Incidence of Incisional Hernia After Stoma Closure Using a Prophylactic Mesh". Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/clinical/NCT04510558. Licensed CC0.

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