Trials / Completed
CompletedNCT01784822
Zenapro™ Hybrid Hernia Repair Device for Ventral Hernia Repair
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 63 (actual)
- Sponsor
- Cook Group Incorporated · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
The objective this study is to collect post-market data on the performance of the Zenapro™ Hybrid Hernia Repair Device when used to reinforce or bridge the abdominal wall for the repair of ventral hernias.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Zenapro™ Hybrid Hernia Repair Device | Device will be placed during open or laparoscopic hernia repair. |
Timeline
- Start date
- 2013-02-01
- Primary completion
- 2016-06-01
- Completion
- 2016-06-01
- First posted
- 2013-02-06
- Last updated
- 2017-06-15
Locations
5 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT01784822. Inclusion in this directory is not an endorsement.