# Rebound Hernia Repair Device Mesh Trial

> **NCT00968773** · PHASE4 · UNKNOWN · sponsor: **Minnesota Medical Development, Inc.** · enrollment: 70 (estimated)

## Conditions studied

- Inguinal Hernia

## Interventions

- **DEVICE:** Rebound HRD
- **DEVICE:** Standard hernia mesh (VitaMesh)

## Key facts

- **NCT ID:** NCT00968773
- **Lead sponsor:** Minnesota Medical Development, Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2009-09
- **Primary completion:** 2012-03
- **Final completion:** 2013-09
- **Target enrollment:** 70 (ESTIMATED)
- **Last updated:** 2016-03-15

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00968773

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00968773, "Rebound Hernia Repair Device Mesh Trial". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT00968773. Licensed CC0.

---

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