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Management of DUSHIVISHAJANYA VYANGA through VARNAKA GHRITA AND VARNYA MAHAKASHAYA ALONG WITH ORAL ADMINISTRATION OF SHIRISH CHURNA

EFFICACY OF EXTERNAL APPLICATION OF VARNAKA GHRITA AND VARNYA MAHAKASHAYA ALONG WITH ORAL ADMINISTRATION OF SHIRISH CHURNA IN DUSHIVISHAJANYA VYANGA WITH SPECIAL REFERENCE TO MELASMA - NILL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/082885
Enrollment
60
Registered
2025-03-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: L00-L99- Diseases of the skin and subcutaneous tissue

Interventions

None listed

Sponsors

Madan mohan malviya government ayurved college udaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with classical sign and symptoms of dushivishajany vyanga. Patients from the age group of 18 to 50 years of either sex.

Exclusion criteria

Exclusion criteria: Hyperpigmentation since birth like Nevus of Ota Age less than 18 years and more than 50 years Dushivishajanya vyanga (melasma) caused due to any systemic disease like Addison s disease, Cushing s syndrome etc. Patients having skin disease like psoriasis, leprosy, acne vulgaris, eczema and leucoderma. hyperpigmentation due to tubercular therapy or malignant cases. Dushivishajanya vyanga (melasma) caused by tumor like malignant melanoma. History of hypersensitivity. Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
Changes in the clinical manifestations of dushivishajanya vyangaTimepoint: 45 days

Secondary

MeasureTime frame
Changes in objective parameters of melasma & QOL (quality of life) of patientsTimepoint: 45 days

Countries

India

Contacts

Public ContactDr Pappu Lal Sharma

Madan Mohan Malviya Government Ayurved College Udaipur

pappulalsharma@gmail.com9783023473

Outcome results

None listed

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