# GORE® ENFORM Biomaterial Product Study

> **NCT04718168** · NA · RECRUITING · sponsor: **W.L.Gore & Associates** · enrollment: 245 (estimated)

## Conditions studied

- Hernia, Ventral
- Hernia, Hiatal
- Hernia, Diaphragmatic
- Incisional Hernia

## Interventions

- **DEVICE:** Gore ENFORM Biomaterial (Preperitoneal)
- **DEVICE:** Gore ENFORM Biomaterial (Intraperitoneal)

## Key facts

- **NCT ID:** NCT04718168
- **Lead sponsor:** W.L.Gore & Associates
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2021-05-17
- **Primary completion:** 2026-09
- **Final completion:** 2026-09
- **Target enrollment:** 245 (ESTIMATED)
- **Last updated:** 2026-02-18


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04718168

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04718168, "GORE® ENFORM Biomaterial Product Study". Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/clinical/NCT04718168. Licensed CC0.

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