Determination of the antiphlogistic effect and the compatibility of herbal cosmetic ointments
Not Applicable
- Conditions
- Patch test on normal skin of healthy volunteers
- Registration Number
- DRKS00017825
- Lead Sponsor
- niversitätsklinikum Freiburg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 43
Inclusion Criteria
Volunteers that fulfill the following inclusion criteria:
•male and female volunteers older than 18 years
•ability to give written informed consent
•ability to adhere to the directions and conditions of the study
Exclusion Criteria
General exclusion criteria
•reduced general condition
•participation in other clinical trials during the last 4 weeks
•volunteers that can not comprehend and adhere to the conditions of the study
specific exclusion criteria
•dermatological skin disorder requiring specific therapy
•known intolerance of any component of the study preparation
•medical co-medication with anti-inflammatory, immuno-modulatory or antibiotic drugs (i.e. antibiotcs, antihistamines, glucocorticoids or immunosuppressive drugs).
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction of the UV induced skin erythema (UV erythema test) by the test preparations in comparison to placebo after 48 h. Skin erythema is measured photometrically after 48 h using a Mexameter.
- Secondary Outcome Measures
Name Time Method Skin tolerability of the test preparations determined in the occlusive patch test on non irradiated skin after 48 h. Skin erythema is measured photometrically after 48 h using a Mexameter.