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

A randomized clinical trial to evaluate the effectiveness of Arjunadi lepa and Naturopathy based face mud pack in vyanga with special reference to melasma.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/042971
Enrollment
40
Registered
2022-06-02
Start date
Unknown
Completion date
Unknown
Last updated
2022-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: L811- Chloasma

Interventions

None listed

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Change in Melasma Area and Severity Index (MASI) Score 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). Timepoint: 8 weeks

Secondary

MeasureTime frame
1. Color assessment of facial hyperpigmentation 2. Patients Global Assessment of facial hyperpigmentation 3. Dermatology life quality indexTimepoint: 8 weeks

Countries

India

Contacts

Public ContactDr Ravi Kumar

National Institute of Ayurveda

drravikumar786@gmail.com9555554077

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026