# Clinical Study on the Safety of SAFIL® MESH

> **NCT04947202** · — · COMPLETED · sponsor: **Aesculap AG** · enrollment: 152 (actual)

## Conditions studied

- Abdominal Wall Defect
- Ventral Hernia
- Abdominal Hernia
- Fascial Hernia

## Interventions

- **DEVICE:** Hernioplasty

## Key facts

- **NCT ID:** NCT04947202
- **Lead sponsor:** Aesculap AG
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2021-07-01
- **Primary completion:** 2021-11-30
- **Final completion:** 2021-11-30
- **Target enrollment:** 152 (ACTUAL)
- **Last updated:** 2022-01-24

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04947202

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04947202, "Clinical Study on the Safety of SAFIL® MESH". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT04947202. Licensed CC0.

---

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