None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Gender: Non-pregnant, non-lactating female aged between 18 to 45, with female:male ratio as 80:20 2. Subject with mild to moderate Dandruff 3. Subject willing to give written informed consent 4. Women of child bearing potential must have a negative urine pregnancy test 5. 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. 6. 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 Scalp Dryness/ Hydration 2. Scalp Sebum 3. Dandruff AssessmentTimepoint: Time Points: At T0, T60min, T+3days, T+7days | — |
Secondary
| Measure | Time frame |
|---|---|
| SGATimepoint: At t0 and t7days | — |
Countries
India
Contacts
CCFT Laboratories