Laparoscopic and Open Ventral Hernia Repair Using the Intramesh T1
NCT01816867 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 96
Last updated 2015-05-22
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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