Trials / Completed
CompletedNCT01364233
Safety Study of MotifMESH (cPTFE) in Abdominal Surgery
A Prospective Outcome Study of Condensed Fenestrated PTFE Mesh (MotifMESH) in Non-sterile Abdominal Wall Defects
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 10 (actual)
- Sponsor
- Medline Industries · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study will monitor surgically repaired large abdominal hernias requiring condensed fenestrated polytetrafluoroethylene mesh (cPTFE).
Detailed description
cPTFEi s a mesh-like product designed to reduce associated post surgical complications.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | MotifMESH | Polytetrafluoroethylene (cPTFE) macroporous mesh |
Timeline
- Start date
- 2011-05-01
- Primary completion
- 2014-03-01
- Completion
- 2014-03-01
- First posted
- 2011-06-02
- Last updated
- 2019-02-26
- Results posted
- 2018-12-04
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01364233. Inclusion in this directory is not an endorsement.