Effect of visible light on skin barrier recovery
Completed
- Conditions
- Skin barrier recovery
- Registration Number
- NL-OMON20423
- Lead Sponsor
- Philips Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 44
Inclusion Criteria
Age between 18 and 40 years;
- Subject must be willing to give a written informed consent;
Exclusion Criteria
- Diagnosis of histamine hypersensitivity;
- Predisposition to respond allergic (including diagnosis of allergy to silver or to other device-related material);
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Measurement of Transepidermal Water Loss (TEWL) at baseline and at 1 hour, 24 hours and 72 hours after tape stripping.
- Secondary Outcome Measures
Name Time Method Measurement of a* value at baseline and at 30 minues and 1h hour after histamine iontophoresis