Clinical Trials Directory

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

TypeNameDescription
DEVICEHelicollHelicoll Collagen I Wound Dressing
DEVICEStandard of Care DressingsStandard 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.

Treatment of Chronic and Non-Chronic Wounds in Patients With Recessive Dystrophic Epidermolysis Bullosa Using Helicoll C (NCT01716169) · Clinical Trials Directory