# Comparative Study of Safety and Efficacy of Heavyweight and Partially Absorbable Mesh in Inguinal Hernia Repair

> **NCT01877122** · PHASE4 · COMPLETED · sponsor: **Samyang Biopharmaceuticals Corporation** · enrollment: 50 (actual)

## Conditions studied

- Hernia, Inguinal

## Interventions

- **DEVICE:** Proflex® Mesh Mesh implantation
- **DEVICE:** Marlex® Mesh Implant

## Key facts

- **NCT ID:** NCT01877122
- **Lead sponsor:** Samyang Biopharmaceuticals Corporation
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2013-04
- **Primary completion:** 2014-12
- **Final completion:** 2014-12
- **Target enrollment:** 50 (ACTUAL)
- **Last updated:** 2015-06-25


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01877122

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01877122, "Comparative Study of Safety and Efficacy of Heavyweight and Partially Absorbable Mesh in Inguinal Hernia Repair". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT01877122. Licensed CC0.

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