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To see the effect of Virechana Karma with Kashmaryadi Kashaya and Eranda Taila in Vatarakta(Gouty Arthritis)

A comparative clinical evaluation of Virechana Karma with Kashmaryadi Kashaya and Eranda Taila in Vatarakta(Gouty Arthritis) - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/074794
Enrollment
40
Registered
2024-10-07
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: M258- Other specified joint disorders

Interventions

None listed

Sponsors

Patanjali Bhartiya Ayurvigyan Evum Anusandhan Sansthan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient present with clinical features of Vatarakta. 1.Patient of either sex between age group of 18 to 60 years. 2.Patients were selected irrespective of sex, occupation, socio economic status, religion etc. 3. Patient fit for Virechana Karma. 4. Patient showing uric acid level above 7mg/dl.

Exclusion criteria

Exclusion criteria: 1. Patients below the age of 18 years and above 60 years were excluded. 2. Patient with metabolic disorder, hypertension, systemic disorders, autoimmune diseases, any endocrine disorder and any other malignancy. 3. Patient with infection and communicable disease. 4. Patients who are pregnant and lactating mother. 5. Patient associated with Rheumatoid arthritis, osteoarthritis. 6. Patient with anorectal diseases like fistula and hemorrhoids.

Design outcomes

Primary

MeasureTime frame
1. Arti (Pain) 2. Stabhdhata (Stiffness) 3. Svathu (Swelling) 4. Daha (Burning) 5. Vaivarnya (Discoloration)Timepoint: 10,30 days

Secondary

MeasureTime frame
Objective parameter 1. CBC with ESR 2. Serum uric acidTimepoint: 10, 30 days

Countries

India

Contacts

Public ContactAkansha Singh

Patanjali Bhartiya Ayurvigyan evum Anusandhan Sansthan Haridwar Uttarakhand

shivani.mahajan@divyayoga.com9760376761

Outcome results

None listed

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