Trials / Completed
CompletedNCT01716169
Treatment of Chronic and Non-Chronic Wounds in Patients With Recessive Dystrophic Epidermolysis Bullosa Using Helicoll Collagen Dressings Versus Standard of Care
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 10 (actual)
- Sponsor
- Stanford University · Academic / Other
- Sex
- All
- Age
- 7 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to test the effectiveness of Helicoll (a collagen wound dressing) in treating chronic and non-chronic wounds of recessive dystrophic epidermolysis bullosa (RDEB) patients. Helicoll will be compared to standard wound dressings.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Helicoll | Helicoll Collagen I Wound Dressing |
| DEVICE | Standard of Care Dressings | Standard of Care wound dressings (e.g. Vaseline gauze) |
Timeline
- Start date
- 2012-10-01
- Primary completion
- 2013-11-01
- Completion
- 2013-11-01
- First posted
- 2012-10-29
- Last updated
- 2016-05-05
- Results posted
- 2016-05-05
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01716169. Inclusion in this directory is not an endorsement.