Laparoscopic and Open Ventral Hernia Repair Using the Intramesh T1

NCT01816867 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 96

Last updated 2015-05-22

No results posted yet for this study

Summary

The purpose of the registry is to evaluate safety and efficacy of the Intramesh T1. This registry will collect data from 100 patients treated for a ventral hernia repair.

Conditions

  • Ventral Hernia

Interventions

DEVICE

Intramesh T1 implantation

Sponsors & Collaborators

  • be Medical

    lead INDUSTRY

Principal Investigators

  • Kurt Van der Speeten, MD, PhD · Ziekenhuis Oost-Limburg

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2014-10-31
Completion
2014-10-31

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01816867 on ClinicalTrials.gov