None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Healthy male or female subjects aged 18 45 years 2. Presence of visible terminal hair in the selected test area 3. Willingness to comply with study procedures 4. Signed Informed Consent Form (ICF) 5. Women of child bearing potential must have a negative urine pregnancy test prior to study entry. 6. Are free of any systemic or dermatologic disorder, which, in the opinion of the investigator, will interfere with the study results or increase the risk of adverse events. 7. 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.Active skin disease or infection at the test site 2.History of hypersensitivity to cosmetic products 3.Use of hair growth inhibitors or laser hair removal in the past 3 months 4.Pregnant or lactating women 5.Participation in another clinical study within 30 days.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Change in hair density 2. Change in Hair Thickness 3. Change in Hair SoftnessTimepoint: At Day 0, Day 14 and Day 28 | — |
Secondary
| Measure | Time frame |
|---|---|
| Not ApplicableTimepoint: Not Applicable | — |
Countries
India
Contacts
CCFT Laboratories