A Clinical Study to Evaluate the Efficacy, Safety and Consumer Perception of a Moisturizing Product
- Conditions
- sensitive skin
- Registration Number
- JPRN-UMIN000047956
- Lead Sponsor
- ION CORPORATIO
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 35
Not provided
a) Female subject is pregnant, nursing, planning a pregnancy, or not using adequate birth control; b) Subject experiences repeated scratching that may cause raised areas on the skin which may bleed or become inflected due to the intense nature of the itch; c) Subject has hives; d) Subject has dense hair on the lower legs; e) Subject is a regular user of prescription itch relievers; f) Subject has used cosmetic itch relievers on the lower legs within one week prior to study start date; #VALUE! h) Subject has known allergies to cosmetics or toiletry products; i) Subject exhibits sunburn, rashes, scratches, burn marks, etc. on the test sites, or has tattoos or piercings which might interfere with study evaluations; j) Subject exhibits or reports a history of acute or chronic dermatological, medical, and/or physical conditions that would preclude application of the test material and/or could influence the outcome of the study; k) Subject has participated in a clinical study which involved the legs within one week of study initiation; l) Subject has a history of skin cancer, or is currently undergoing treatment for active cancer of any kind; m) Subject has diabetes.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method