None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Voluntary men and women between 18 and 55 years of age. 2. 32 particpants with Post Inflammatory Hyperpigmentation (any inflammation causing a blemish, for eg acne). 3. Presenting healthy skin on test sites. 4. Participant willing to provide written informed consent to participate in the study after all information concerning the study procedures and objectives has been explained. 5. Participant ready to comply with study procedures for the duration of the study
Exclusion criteria
Exclusion criteria: 1. Pregnant women by UPT, Lactating mothers. 2. Allergic to any cosmetic product. 3. A participant who the Investigator feels will not be compliant with study requirements. 4. Any type of skin disorder which Investigator feels will interfere with the study 5. Participants on any medical treatment either systemic or topical which may interfere with the performance of the study treatment (presently or in the past 1 month). E.g. topical steroids.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Measurement of skin pH using skin ph meter. 2. Measurement of skin hydration using MMSC 3. Evaluation of Transepidermal Water Loss using VapoMeter. 4. Measurement of skin radiance using glossmeter 5. Evaluation of pore cleansing efficacy using 3D Imaging (On 30 participants with oily skin). 6. Evaluation of skin spot/pigmentation using 3D Imaging. (On 30 participants). 7. Consumer feedback questionnaireTimepoint: Baseline, 15 mins, Day 15 | — |
Secondary
| Measure | Time frame |
|---|---|
| Clinical evaluation for skin intolerancesTimepoint: Day 15 | — |
Countries
India
Contacts
Dr Reddys Laboratories Limited