Effect of ayurvedic lepa preparations in the management of melasma(vyanga).
- Conditions
- Health Condition 1: L811- Chloasma
- Registration Number
- CTRI/2021/04/032828
- Lead Sponsor
- ational institute of ayurveda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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.
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction in classical signs and symptoms of vyaá¹?ga.Timepoint: 45 days
- Secondary Outcome Measures
Name Time Method Better quality of life.Timepoint: 45 days