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To study the concept of seven Dravya in cause and subsequent development of Eka Kushtha and its principle management with special reference to blood letting with Jalauka

To study the concept of Sapta Dravya Samgrah in aetiopathogenesis of Eka Kushtha and its Saiddhantik Chikitsa (principle management) w.s.r. to Jalaukavacharna

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043034
Enrollment
20
Registered
2022-06-06
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: L400- Psoriasis vulgaris

Interventions

None listed

Sponsors

Rajiv Gandhi Ayurvedic college and Hospital Paprola district kangra
Lead Sponsor
Head of the department
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patients showing sign and symptoms of Eka Kushtha (psoriasis). 2) Age group 16-70 years should be included in the trial. 3) Patients willing for trial will be included in the study after obtaining detailed in formed consent.

Exclusion criteria

Exclusion criteria: a. Patients suffering from Anemia, Haemophillia A, Haemophillia B, Septic disorders, Allergic reaction to (Hirudin) active ingredient in leech saliva, Immunocompromised, Hypertension, Diabetes-mellitus, Hepatitis B. b. Patients below 16 year and above 70 year of age. C. Patients not willing for trial.

Design outcomes

Primary

MeasureTime frame
1. Area of Involvement- The body is divided into four sections - Head (10% of a persons skin), arms (20%), trunk (30%) and legs (40%). Each of these area is scored and then four scores are combined into final PASI. 2. Within each area the severity is estimated by three clinical signs: Erythema, Induration, Desquamation.Timepoint: 2 month

Secondary

MeasureTime frame
Cured: 100% relief in signs and symptoms. Marked improvement: More than 75% improvement in signs and symptoms will be recorded as marked improvement. Moderate improvement: 51% to 75% improvement in signs and symptoms will be considered as moderate improvement. Mild improvement: 25% to 50% improvement in sign and symptoms will be considered as mild improvement. No improvement: Less than 25% reduction in signs and symptoms will be noted as unchanged.Timepoint: 3month

Countries

India

Contacts

Public ContactDiksha ayri

Rajiv Gandhi Ayurvedic College and Hospital Paprola

satishgandharve@gmail.com7018241280

Outcome results

None listed

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