# ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention

> **NCT03912662** · NA · TERMINATED · sponsor: **Medtronic - MITG** · enrollment: 32 (actual)

## Conditions studied

- Incisional Hernia

## Interventions

- **DEVICE:** Mesh augmented reinforcement

## Key facts

- **NCT ID:** NCT03912662
- **Lead sponsor:** Medtronic - MITG
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2019-09-18
- **Primary completion:** 2022-09-12
- **Final completion:** 2022-09-12
- **Target enrollment:** 32 (ACTUAL)
- **Why stopped:** Surgical complications arose early in the study, mainly due to patient complexity, not to study device or implantation. Despite refining protocol to exclude highly complex patients, these issues persisted, leading to the study's early termination.
- **Last updated:** 2025-12-03


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03912662

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03912662, "ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention". Retrieved via MORVS 2026-10-23 from https://api.morvs.ai/clinical/NCT03912662. Licensed CC0.

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