Trials / Terminated
TerminatedNCT01834339
EVPOME Versus AlloDerm in Subjects Reconstructed With Large Defect Mandibular Resection
A Randomized, Parallel-Group (Autogenous EVPOME Versus AlloDerm Without Incorporation of Keratinocytes) Study in Subjects Reconstructed With Large Defect Mandibular Resection in Need of Vestibuloplasty for Dental Rehabilitation
- Status
- Terminated
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 1 (actual)
- Sponsor
- Stephen E. Feinberg · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the safety and effectiveness of performing oral reconstructive surgeries using either AlloDerm, a product commonly used for this purpose, or AlloDerm that has been overlaid with the subject's oral mucosal cells and developed into a type of graft that is called an ex vivo produced oral mucosal equivalent, EVPOME.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | AlloDerm | |
| BIOLOGICAL | EVPOME |
Timeline
- Start date
- 2013-09-01
- Primary completion
- 2014-11-01
- Completion
- 2015-12-01
- First posted
- 2013-04-17
- Last updated
- 2017-11-22
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01834339. Inclusion in this directory is not an endorsement.