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Not listed Phase 4 Interventional Accepts healthy volunteers

Rebound Hernia Repair Device Mesh Trial

ClinicalTrials.gov ID: NCT00968773

Public ClinicalTrials.gov record NCT00968773. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 6:04 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Rebound Hernia Repair Device Trial

Study identification

NCT ID
NCT00968773
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Minnesota Medical Development, Inc.
Industry
Enrollment
70 participants

Conditions and interventions

Interventions

  • Rebound HRD Device
  • Standard hernia mesh (VitaMesh) Device

Device

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2009
Primary completion
Feb 29, 2012
Completion
Aug 31, 2013
Last update posted
Mar 14, 2016

2009 – 2013

United States locations

U.S. sites
2
U.S. states
2
U.S. cities
2
Facility City State ZIP Site status
University of Kentucky Dept. Of Surgery Lexington Kentucky 40536-0293
The Ohio State Medical Center, Dept. of Surgery Columbus Ohio 43210-1228

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00968773, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 14, 2016 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00968773 live on ClinicalTrials.gov.

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