None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Voluntary men and women between 16 and 30 years of age (approximately equal number). 2. Having mild to moderate active acne or Non-cystic acne. 3. Not on any treatment for acne. 4. Accepting not to use products with the same end benefit during the entire study duration. 5. Cooperating, informed of the need and duration of the examinations, and ready to comply with protocol procedures. 6. Having signed a Consent Form and will be once informed orally and in writing of all information concerning the study procedures and study objectives.
Exclusion criteria
Exclusion criteria: 1.Pregnancy by history and lactating women. 2. Premenstrual women and women on oral contraceptives. 3. Skin allergy antecedents or atopic subject. 4. Hypersensitivity to any cosmetic product, raw material. 5. PCOD, hirsutism, any hormonal issues etc by history or clinical examination. 6. For whom the Investigator considers that he/she will not be compliant with study procedures. 7. Any clinically significant systemic or cutaneous disease, which may interfere with study treatments or procedures. 8. 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). 9. Participant in an exclusion period or already participating in another similar cosmetic or therapeutic trial as identified during screening on visit 1 (V1).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of Acne lesions and redness by Clinical evaluation, Instrumentation and Self evaluation.Timepoint: Day 0, 72 hours, Day 7, Day 21 | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of tolerance of the test productTimepoint: Day 0, 72 hours, Day 7, Day 21 | — |
Countries
India
Contacts
PhytoMyco Research Pvt. Ltd.