None listed
Conditions
Interventions
Intervention1: Body Lotion: Fixed amount of test product will be applied to the skin, then spread over the whole test site using a finger cot. Single application
Control Intervention1: Reference Stand
Sponsors
Zydus Wellness Products Limited
Eligibility
Inclusion criteria
Inclusion criteria: 1) Healthy adult males and non-pregnant/non-lactating females. 2) Participants with ITA value of at least 28 using Chromameter and be untanned on the test area. 3) Participants with uniform skin color over the whole test area and with no variation in ITA greater than 5 from each other or the MEDu test area. 4) Participants with test sites, free from pigmentation, nevi, sunburn and hair.
Exclusion criteria
Exclusion criteria: 1) Participants with a history of abnormal responses to the sun (e.g., phototoxic or photoallergic responses). 2) Participants having marks, blemishes or nevi in the test area. 3) Participants presenting existing sun damage in the test area. 4) Participants who had sun exposure on their back within the eight weeks leading up to the SPF testing. 5) Participants having skeletal protrusions and extreme areas of curvature in the test area.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in Individual Minimal Erythema Dose (iMED) ScoreTimepoint: Day 1 | — |
Secondary
| Measure | Time frame |
|---|---|
| Delayed Erythema ResponseTimepoint: Day 2 | — |
Countries
India
Contacts
Public ContactDr Parth Joshi
Cliantha Research
Outcome results
None listed