Investigation on the effect of topical application of a verum formulation on wound healing in a double-blind placebo-controlled study.
- Conditions
- Epidermal und DermaleWound Healing after laser ablation
- Registration Number
- DRKS00031896
- Lead Sponsor
- COTY LANCASTER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 12
Who are older than 40 years old
- Who have no known skin diseases
- who have a skin type of I-III (Fitzpatrick)
- Who have been informed about the aims of the study and the nature of the investigations.
- who have given their informed consent to participate in writing.
- who have not received intensive sun exposure on the skin areas to be irradiated on the forearm within the last 14 days before the irradiation date.
- Minors
- nursing mothers and women with known pregnancy
- Known skin diseases
- Skin type >III (Fitzpatrick)
- past ablative or peeling treatments of the forearm
- intensive sun exposure on the skin areas to be measured on the forearm within the last 14 days before the irradiation date
- Persons who cannot make decisions on their own responsibility
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Diameter of micro-wounds measured with the LSM are smaller with the verum cream.
- Secondary Outcome Measures
Name Time Method Wound treated with verum cream heals better assessed by the clinic dermatologist