None listed
Conditions
Interventions
Intervention1: Efficacy study of anti-acne lotion: This is efficacy study of three samples of anti-acne lotion. Each sample will apply on three different groups. Each group will have ten volunteers. E
Sponsors
NIKKOL GROUP COSMOS TECHNICAL CENTER CO LTD
Eligibility
Inclusion criteria
Inclusion criteria: Phototype III to V. Healthy skin on test area. Acne clearly visible on face. Not undergone any type of treatment on ACNE VULGARIS since last three months. having signed a consent form able to read and write valid id prrof. urine test negative for women.
Exclusion criteria
Exclusion criteria: 1.Pregnant/nursing mothers. 2. Scars, excessive terminal hair or tattoo on the studied area. 3. Henna tattoo anywhere on the body (in case of studies involving hair dyes). 4. Dermatological infection/pathology on the level of studied area. 5. Hypersensitivity, allergy antecedent (to any cosmetic product, raw material or hair dye). 6. Any clinically significant systemic or cutaneous disease, which may interfere with study treatment or procedures. 7. Chronic illness which may influence the outcome of the study. 8. Subjects 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. Subjects in an exclusion period or participating in another food or cosmetic or therapeutic trial. 10. Undergone any type of treatment on ACNE VULGARIS since last three months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| to improve Acne on face using Acne Recovery Lotion on human subjectTimepoint: 28 days | — |
Secondary
| Measure | Time frame |
|---|---|
| To check the improvement of acne vulgaris after the application of ACNE RECOVERY LOTION.Timepoint: 28 DAYS | — |
Countries
India
Contacts
Public ContactSAMEER P SHINDE
Sanity Lifesciences Pvt.. Ltd.
Outcome results
None listed