Trials / Terminated
TerminatedNCT00820040
Feasibility of Permacol Use in Infected Fields
To Examine the Feasibility of Using Permacol® Surgical Implant in the Repair of Abdominal Wall Defects After Removal of Chronic Infect Prosthetic Mesh
- Status
- Terminated
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 10 (actual)
- Sponsor
- Medtronic - MITG · Industry
- Sex
- All
- Age
- 18 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
This pilot study is to examine the feasibility of using Permacol Surgical Implant in the repair of abdominal wall defects after removal of infected prosthetic mesh
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | acellular porcine dermal collagen mesh | porcine mesh for hernia repair/ abdominal wall reconstruction |
Timeline
- Start date
- 2009-07-01
- Primary completion
- 2011-08-01
- Completion
- 2011-08-01
- First posted
- 2009-01-09
- Last updated
- 2020-12-09
- Results posted
- 2020-12-09
Locations
3 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00820040. Inclusion in this directory is not an endorsement.