Evaluation de la tolérance d'un produit cosmétique dans les suites de séances de photothérapie dynamique
- Conditions
- The subjects who will participate in the clinical study will have actinic keratoses and/or superficial basal cell carcinoma that need to be treated by dynamic phototherapy.
- Registration Number
- EUCTR2010-019788-12-BE
- Lead Sponsor
- aboratoire BIODERMA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Authorised-recruitment may be ongoing or finished
- Sex
- All
- Target Recruitment
- Not specified
- Subject aged of more than 18 years.
- Subject who has to make dynamic phototherapy session to treat actinic keratosis and/or superficial basal cell carcinoma.
- Subject who has accepted not to be exposed to UV during the whole study and at least 3 months after the end of the study.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range
- Pregnant or breast-feeding women.
- Subject with cutaneous or medical illness that might prevent the subject to be included in the study, according to the investigator.
- Documented allergies to study product components.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method