# Progrip Ventral Study for Sublay Repair

> **NCT01622127** · — · COMPLETED · sponsor: **University Hospital, Ghent** · enrollment: 55 (actual)

## Conditions studied

- Primary Ventral and Incisional Hernia Repair

## Interventions

- **DEVICE:** Parietex ProGrip™

## Key facts

- **NCT ID:** NCT01622127
- **Lead sponsor:** University Hospital, Ghent
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2012-02
- **Primary completion:** 2015-06
- **Final completion:** 2023-12-31
- **Target enrollment:** 55 (ACTUAL)
- **Last updated:** 2024-06-03

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01622127

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01622127, "Progrip Ventral Study for Sublay Repair". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT01622127. Licensed CC0.

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