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A Comparative Pharmaco-Clinical Study of Palash and Chakramarda in the managenant of Dadru kustha

A Comparative Pharmaco-Clinical Study of Palash (Butea monosperma Lam.kuntze) and Chakramarda (Cassia tora Linn) in the managenant of Dadru kustha - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091275
Enrollment
40
Registered
2025-07-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: B359- Dermatophytosis, unspecified

Interventions

None listed

Sponsors

Pt.khushi lal sharma government Autonomus Ayurveda collage and institute science bhopal mp
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Individuals aged between 21-50 years without any discrimination of gender, caste, and religion, Patients fulfilling the diagnostic criteria. Individuals having clinical sign and symptoms of Dadru roga according to Ayurvedic classics. Individuals who will give written consent for the study.

Exclusion criteria

Exclusion criteria: Pregnancy and Lactating mothers. Subject having skin disorder other than Dadru. Immunocompromised patient (HIV, T.B.,) other complicated disorder uncontrolled diabetes, skin cancer, psoriasis, malignant of skin diseases, Generalized eczema, hansen s disease, cellulitis and other autoimmune disease Patient who used to Immunosuppressive drugs.

Design outcomes

Primary

MeasureTime frame
the reduction or elimination of symptoms like itching (Kandu), redness (Raga), eruptions (Pidika), and elevated circular skin lesions (Utsanna Mandala). Successful treatment aims to alleviate these symptoms and prevent recurrence.Timepoint: 7 week

Secondary

MeasureTime frame
Complete Blood Count (CBC) RBSTimepoint: 45 days

Countries

India

Contacts

Public ContactDrAjay kurmi

pt khushilal sharma ayurveda collage bhopal

Sharmavinod389@gmail.com9926379195

Outcome results

None listed

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