# Comparison of Two Mesh/Fixation Concepts for Laparoscopic Ventral and Incisional Hernia Repair

> **NCT02233569** · NA · TERMINATED · sponsor: **Polish Hernia Study Group** · enrollment: 50 (actual)

## Conditions studied

- Hernia, Abdominal
- Hernia,Ventral

## Interventions

- **PROCEDURE:** Intraperitoneal onlay mesh (IPOM) repair with the use of Phisiomesh implant and Securestrap fixation device.
- **PROCEDURE:** Intraperitoneal onlay mesh (IPOM) repair with the use of Ventralight ST implant with SorbaFix fixation device.
- **DEVICE:** Ventralight ST implant
- **DEVICE:** ETHICON PHYSIOMESH®

## Key facts

- **NCT ID:** NCT02233569
- **Lead sponsor:** Polish Hernia Study Group
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2012-11
- **Primary completion:** 2014-02
- **Final completion:** 2014-02
- **Target enrollment:** 50 (ACTUAL)
- **Why stopped:** The high recurrence rate and the findings during the reoperations were considered as serious adverse events and were the reason for study termination.
- **Last updated:** 2014-09-08


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02233569

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02233569, "Comparison of Two Mesh/Fixation Concepts for Laparoscopic Ventral and Incisional Hernia Repair". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT02233569. Licensed CC0.

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