# Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application

> **NCT05094089** · — · ACTIVE_NOT_RECRUITING · sponsor: **W.L.Gore & Associates** · enrollment: 320 (estimated)

## Conditions studied

- Hernia, Ventral
- Hernia Incisional
- Hernia Incisional Ventral

## Interventions

- **DEVICE:** Hernia repair with mesh

## Key facts

- **NCT ID:** NCT05094089
- **Lead sponsor:** W.L.Gore & Associates
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** ACTIVE_NOT_RECRUITING
- **Start date:** 2023-02-24
- **Primary completion:** 2030-07-31
- **Final completion:** 2030-07-31
- **Target enrollment:** 320 (ESTIMATED)
- **Last updated:** 2026-01-21


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05094089

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05094089, "Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application". Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/clinical/NCT05094089. Licensed CC0.

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