Health Condition 1: L700- Acne vulgaris
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Gender: Non-pregnant, non-lactating female aged between 18 to 34 2. Subject willing to give written informed consent 3. Women of child bearing potential must have a negative urine pregnancy test 4. Free of any systemic and dermatologic disorder, which in the opinion of the investigator, will interface with the study results or increase the risk of AE. 5. Are willing to avoid prolonged exposure of the treatment area to ultraviolet radiation (natural or artificial) for the duration of the study.
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. 6.Have a known sensitivity to any of the constituents of the test product including sensitivities to any of the constituents. 7. Have used, are using, or are planning to use immunosuppressive or immunomodulatory medications (i.e., biologics), including corticosteroids. 8. Have a history of alcohol or illegal drug/ substance abuse or suspected alcohol or illegal drug/substance abuse in the past 2 years.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Change in percentage of consumers achieved a visible even tone skin/texture in 30 days. 2. Change in percentage of volunteers achieved a visibly brighter skin in 30 days. 3. Change in percentage of volunteers achieved a glowing skin in 30 days. 4. Change in percentage of volunteers experienced visible reduction of dark spot/ hyperpigmentation in 30 days 5. Change in percentage of volunteers experienced how much percentage of improvement in skin tone/texture.Timepoint: Day14, Day 28 | — |
Secondary
| Measure | Time frame |
|---|---|
| Not applicableTimepoint: Not applicable | — |
Countries
India
Contacts
CCFT Laboratories