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Trials / Completed

CompletedNCT00622583

International Hernia Mesh Registry

A Two-Year Follow-up, Post-Implantation, Multi-center, International Hernia Mesh Registry

Status
Completed
Phase
Study type
Observational
Enrollment
5,179 (actual)
Sponsor
Ethicon, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is an open-label, multi-center, long-term, prospective hernia mesh registry. A minimum of 4,800 hernia patients will be enrolled from approximately 60 active sites globally

Detailed description

Patients will be followed for 2-years post-implantation, in a post-market setting to help identify best practices leading to lower recurrence rates and decreases in chronic pain, associated with the hernia repair procedure.

Conditions

Timeline

Start date
2007-09-01
Primary completion
2019-04-24
Completion
2021-01-25
First posted
2008-02-25
Last updated
2023-06-05

Locations

54 sites across 13 countries: United States, Australia, Belgium, Canada, China, France, Germany, Italy, Netherlands, South Africa, Spain, Sweden, United Kingdom

Source: ClinicalTrials.gov record NCT00622583. Inclusion in this directory is not an endorsement.

International Hernia Mesh Registry (NCT00622583) · Clinical Trials Directory