Burn Wound Clinical Trial
— keratinocyteOfficial title:
Clinical Study for Evaluation of Clinical Efficacy and Safety of Autologous Cultured Keratinocyte Cell on Severe Burn Wood
Verified date | September 2009 |
Source | Modern Cell and Tissue Technology |
Contact | n/a |
Is FDA regulated | No |
Health authority | Korea: Food and Drug Administration |
Study type | Interventional |
The efficacy and safety of Autologous cultured keratinocyte cell on severe burn wound.
Status | Enrolling by invitation |
Enrollment | 19 |
Est. completion date | January 2010 |
Est. primary completion date | May 2008 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 1 Year to 70 Years |
Eligibility |
Inclusion Criteria: - Age : 1~70 years - More than 30% TBSA of second degree burn or more than 10% TBSA of third degree burn - Must provide signed informed consent prior to participation in any study-related procedures Exclusion Criteria: - Have a pyogenic infection - Part of the facial cosmetic surgery cost - Hypersensitivity reactions in patients with bovine proteins - Hypersensitivity reactions in patients with Gentamycin - Pregnancy or lactation |
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Hangang Sacred Heart Hospital | Seoul |
Lead Sponsor | Collaborator |
---|---|
Modern Cell and Tissue Technology |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | engraftment assessment | 4week | Yes | |
Secondary | the vancouver burn scar scale | 8, 12, 24 week | Yes |
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