Health Condition 1: L811- Chloasma
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Subjects of either sex with age group above 18 years will be selected. 2.Subjects with Fitzpatrick skin types III, IV and V presenting with the classical signs and symptoms of Vyaá¹?ga(melasma) will be selected. 3.Subjects willing to participate in the study and willing to give written informed consent will be selected by explaining the interventions in detail. 4.Female subjects of childbearing potential using a reliable from of contraception during the course of the study excluding oral contraceptive pills at the time of the study or in the past 6 months (intrauterine device or condoms) or female of nonchildbearing potential (hysterectomy, bilateral ovariectomy or tubal section/ligation). 5.Female subjects of childbearing potential with a negative urine pregnancy test before inclusion in the study.
Exclusion criteria
Exclusion criteria: 1.Hyperpigmentation caused since birth like nevus of ota. 2.Hyperpigmentation caused by tumor like malignant melanoma. 3.Vyaá¹?ga along with other kuá¹£á¹ha roga to be excluded. 4.Pregnant women, nursing mothers. 5.Subjects suffering from other pigmentation disorders. 6.Subject having used any cosmetic depigmenting agent within 2 weeks prior to inclusion. 7.Subjects who have used a topical or inhaled corticosteroid or systemic steroids within 1 month prior to inclusion in the study. 8.Subjects having used topical tretinoin within 3 months or topical hydroquinone within 6 months prior to inclusion. 9.Subjects with history of endocrinopathies.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in classical signs and symptoms of vyaá¹?ga.Timepoint: 45 days | — |
Secondary
| Measure | Time frame |
|---|---|
| Better quality of life.Timepoint: 45 days | — |
Countries
India
Contacts
National institute of ayurveda jaipur