None listed
Conditions
Interventions
Intervention1: CL-TRFW-25: Approx. 1 gm of product will be applied twice a week during the entire study duration.
Control Intervention1: NIL: NIL
Sponsors
Zydus Wellness Products Limited
Eligibility
Inclusion criteria
Inclusion criteria: 1) Non-pregnant /non-lactating females. 2) Participants with fitzpatrick skin type IV and V. 3) Participants with visible skin tan on face, at least 2 shade darker than a Sun protected upper volar arm. 4) Participants with visible blackheads on the face. 5) Participants with at least 2 blemishes. 6) Participants who are willing to voluntarily participate in the study and provide signed informed consent.
Exclusion criteria
Exclusion criteria: 1) Participants with dark facial skin as determined by dermatologist. 2) Participants having any active dermatological skin diseases (e.g., psoriasis, atopic dermatitis, rosacea etc.), that might interfere with clinical assessments. 3) Participants using any other facewash during the study period. 4) Participants using other marketed skin lightening products during the study period or in the past 6 weeks. 5) Participants who are receiving topical or systemic treatments for pigmentation within the last 30 days. 6) Participant undergoing treatment for Seborrhoea, Acne, Dermatitis, Melasma, Lentigines, skin Lightening/ any other cosmetic/ dermatologic skin condition on face.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the efficacy of test product on tanned skin, based on instrumental evaluations.Timepoint: Day 01 (Before and after product usage) , Day 03, Day 07, Day 14 and Day 21. | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the efficacy of test product on tanned skin, based on clinical, instrumental and subjective evaluations.Timepoint: Day 01 (Before and after product usage) , Day 03, Day 07, Day 14 and Day 21. | — |
Countries
India
Contacts
Public ContactDr Parth Joshi
Cliantha Research
Outcome results
None listed