None listed
Conditions
Interventions
None listed
Sponsors
Hindustan Unilever Limited
Eligibility
Inclusion criteria
Inclusion criteria: 1.Healthy females volunteers between 20-45 years of age. 2.Subjects with self perceived dark spot problems. 3.Presence of 2-3 spots on face 4.Volunteer in good health condition as per the medical screening criteria with no disease state or physical condition that the Investigator believes could interfere with the interpretation of the data. 5.Subject free of excessive hair, acne, cuts, abrasions, fissures, wounds, lacerations, or any other active skin conditions on the face. 6.Subject who agree not to use of any other skin lightening product/treatment/soap bar/home remedy on their face during the study period other that the study product provided. 7.Subject who agrees not to carry out bleaching or any other skin care procedures on face during the study 8.Volunteer able to read, understand and sign an appropriate informed consent form indicating her willingness to participate.
Exclusion criteria
Exclusion criteria: 1.Volunteers who participated in a study with face as the target area within 4 weeks of the start of this study or is currently participating in such a study. 2.Volunteer pregnant or planning to become pregnant. 3.Volunteers who are breastfeeding or having stopped to breastfeed in the past three months. 4.Volunteers with any other signs of significant local irritation, erythema or skin disease on face as well as on the visible parts of the body skin site. 5.Volunteers with self-perceived sensitive skin. 6.Volunteers having chronic illness or had major surgery in the last year. 7.Volunteers undergoing any treatment of any skin condition on body. 8.Volunteers taking any oral antibiotic medication currently or within the last 8 weeks. 9.Volunteers taking medication 10.Volunteers taking medication for any condition which the Investigator believes may influence the interpretation of the data. 11.Volunteers on food supplements.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Significant reduction in severity of dark spotsTimepoint: Baseline, 2week, 4 week | — |
Secondary
| Measure | Time frame |
|---|---|
| NilTimepoint: NA | — |
Countries
India
Contacts
Public ContactDr Mohit Lalvani
MASCOT-SPINCONTROL India Pvt. Ltd.
Outcome results
None listed