MedPath

Evaluate the efficacy of Arjunadi lepa and Naturopathy based face mud pack in vyanga.

Phase 2
Conditions
Health Condition 1: L811- Chloasma
Registration Number
CTRI/2022/06/042971
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
Inclusion Criteria

1. Patients suffering from classical clinical signs and symptoms of Vyanga

2. Patient of age 20 to 40 years irrespective of sex and religion

Exclusion Criteria

1.Patients receiving hormone or corticosteroid therapy

2.Patients with history of endocrine disorders or allergies.

3.Patients taking depigmenting or whitening products (oral or topical) within the previous 6 weeks.

4.Pregnant or breast feeding mother

5.Subjects who are allergic to chemical compound in the Lepa or fragrance.

6.Using a medication that increases sensitivity to sunlight including doxycycline, minocycline, tetracycline, ciprofloxin, hydrochlorothiazide, and sulfonamides.

7.Usage of any new skincare products during the course of the study.

8.Facial/laser treatment within the last 3 months

9.Facial cosmetic surgery within the last 12 months

10.Physical skin conditions such as excessive hair, scarring, tattoos that might impair evaluations of the test sites

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in Melasma Area and Severity Index (MASI) Score <br/ ><br>Severity of melasma in each of the four regions (forehead, right malar region, left malar region and chin) is assessed on percentage of the total area involved (A), darkness (D), and homogeneity (H). <br/ ><br>Timepoint: 8 weeks
Secondary Outcome Measures
NameTimeMethod
1. Color assessment of facial hyperpigmentation <br/ ><br>2. Patients Global Assessment of facial hyperpigmentation <br/ ><br>3. Dermatology life quality indexTimepoint: 8 weeks
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