None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Gender: Non-pregnant, non-lactating female Age 18?55 years. 2. Subject willing to give written informed consent 3. Women of child bearing potential must have a negative urine pregnancy test 4. Fitzpatrick skin type II?V. 5. Healthy skin on test areas. 6. Agree to avoid other facial actives 7 days prior to visit.
Exclusion criteria
Exclusion criteria: 1. Subjects who are pregnant, breast feeding, or planning to become pregnant during the study 2. Have any evidence of systematic cancer, squamous cell carcinoma, basal cell carcinoma in the last 5 years, or any other confounding skin condition. 3. Have open sore or open lesions in the treatment area 4. Have any condition that, in the opinion of the investigator, would confound the safety and efficacy assessments of the product. 5. Have participated in any interventional clinical trial in the previous 30 days. Known allergy to product ingredients. 6. Active dermatitis, wounds or lesions on test areas. 7. Facial procedures in prior 4 weeks (e.g., peels, lasers). 8. Systemic retinoids in prior 6 months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. change in skin hydration 2. DSLR Imaging 3. Dermatologist visual grading Timepoint: At T0, 30 minutes, 2 hour and 8 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. SGATimepoint: At T0, 30 minutes, 2 hour and 8 hours | — |
Countries
India
Contacts
CCFT Laboratories