None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Individual should have ITA angle in the range of 18 t0 40, 41 to 55, and greater than 56 2. Individuals free of any dermatological or systemic disorder which would interfere with the results, at the discretion of the investigator. 3. Individuals who have completed a preliminary medical history evaluation. 4. Individuals who have read, understood and signed an informed consent document relating to the specific study to which they are subscribing. 5. Individuals with no known abnormal response to sunlight.
Exclusion criteria
Exclusion criteria: 1. Individual should have ITA angle in the range of 18 t0 40, 41 to 55, and greater than 56 2. Individuals free of any dermatological or systemic disorder which would interfere with the results, at the discretion of the investigator. 3. Individuals who have completed a preliminary medical history evaluation. 4. Individuals who have read, understood and signed an informed consent document relating to the specific study to which they are subscribing. 5. Individuals with no known abnormal response to sunlight.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in Individual MED (iMED) scoreTimepoint: Day1, Day2 , Day3 | — |
Secondary
| Measure | Time frame |
|---|---|
| Not ApplicableTimepoint: Not Applicable | — |
Countries
India
Contacts
CCFT Laboratories