Health Condition 1: L709- Acne, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Subjects with mild to moderate acne condition. OR Subjects who are prone to develop however with no existing acne. 2) Subjects with oily skin having Sebumeter measurement more than 150 (ug/cm2). 3) Subjects with acne marks/spots and post acne scar. 4) Subjects with visible facial pores.
Exclusion criteria
Exclusion criteria: 1) Subjects with drug induced acne as disclosed by subjects. 2) Subjects undergoing treatment for skin lightening or using other marketed skin lightening products during the study period or in the past 6 weeks. 3) Subjects who are receiving topical or systemic treatments for acne, acne marks and acne scars. 4) Subjects receiving medications (e.g., steroids or antihistamines) would compromise the study. 5) Chronic illness which may influence the cutaneous state.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the efficacy of test product on acne or acne prone skin, based on clinical, instrumental and subjective evaluations done at predetermined time points.Timepoint: Day 01 (before application and 15 mins), Day 02 (24hrs), Day 03 (48 hrs), Day 04 (72 hrs), Day 05 (+ 01 day), Day 07 (+ 02 days), Day 15 (+ 02 days) and Day 29 (+ 02 days). | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Cliantha Research