None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Gender: Male and Female with age 18-45 (80:20) 2)Presence of visible lip dryness, dullness or pigmentation. 3)Subjects willing to give written informed consent 4)Women of child bearing potential must have a negative urine pregnancy test prior to study entry. 5. Signed informed consent form
Exclusion criteria
Exclusion criteria: 1. Pregnant or nursing mothers 2. Current dermatological treatments on the lips. 3. Active cold sores, infections, open wounds, or trauma to the lips. 4.Tolerance rating included in the past-treatment questionnaire. 5.volunteers to report and discomfort or adverse events during the study period 6.Any clinically significant systemic or cutaneous disease, which may interfere with study treatment or procedures 7.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)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Change in hydration 2. Change in Melanin 3. DSLR imaging 4. Visual Grading 5. Dermascope imagingTimepoint: At t0, t30min, t28days | — |
Secondary
| Measure | Time frame |
|---|---|
| SGATimepoint: t28days | — |
Countries
India
Contacts
CCFT Laboratories