A Clinical Study to Evaluate Efficacy and Consumer Perception of a Test Material
- Conditions
- sensitive skin
- Registration Number
- JPRN-UMIN000047955
- 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 has eczema on the test sites; c) Subject has a sever itch with noticeable scratch (as determined by the LPN); d) Subject has hives; e) Subject uses a prescription itch reliever; f) Subject has received treatment with sympathomimetics, antihistamines, vasoconstrictors, non-steroidal anti-inflammatory agents, and/or systemic or topical corticosteroids within one week prior to initiation of the study; g) Subject has a history of acute or chronic dermatologic, medical, and/or physical conditions which would preclude application of the test material and/or could influence the outcome of the study; h) Subject is currently taking certain medications which, in the opinion of the Principal Investigator, may interfere with the study; i) Subject has known allergies to skin treatment products or cosmetics, toiletries, and/or topical drugs; j) Subject has a history of skin cancer, or is currently undergoing treatment for active cancer of any kind; k) Subject has insulin-dependent diabetes.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Itch evaluation of Baseline, immediately after application,1 min, 2 min, 5min, 10min, 30min using VAS method.
- Secondary Outcome Measures
Name Time Method