Trials / Completed
CompletedNCT01816867
Laparoscopic and Open Ventral Hernia Repair Using the Intramesh T1
Laparoscopic and Open Ventral Hernia Repair Using the Intramesh T1: a Prospective, Multicenter Registry
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 96 (actual)
- Sponsor
- be Medical · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Intramesh T1 implantation |
Timeline
- Start date
- 2013-01-01
- Primary completion
- 2014-10-01
- Completion
- 2014-10-01
- First posted
- 2013-03-22
- Last updated
- 2015-05-22
Locations
1 site across 1 country: Belgium
Source: ClinicalTrials.gov record NCT01816867. Inclusion in this directory is not an endorsement.