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Effect of Madhuyashtyadi Taila Matra Basti in Patients suffering from Vatarakta (Gout)

A Prospective Open Label Controlled Clinical Study to Determine the Efficacy of Madhuyashtyadi Taila Matra Basti in the Management of Vatarakta with Special Reference to Gout - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/109914
Enrollment
80
Registered
2026-05-04
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: M100- Idiopathic gout

Interventions

None listed

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients indicated for Basti therapy (Basti Arha). 2. Diagnosed cases of Vatarakta presenting with classical features like Sandhishool (pain), Daha (burning sensation), Shotha (swelling), and Stambha (stiffness).

Exclusion criteria

Exclusion criteria: 1. Patients contraindicated for Basti therapy (Basti Anarha). 2. Patients below 30 years or above 60 years of age. 3. Patients of Vatarakta having any chronic systemic disorder which interferes with the present study, such as chronic heart disease, chronic renal disorders, or history of previous intestinal surgery. 4. Pregnant and lactating women. 5. Patients on allopathic uric acid lowering medications and corticosteroids.

Design outcomes

Primary

MeasureTime frame
Vatarakta symptom scoresTimepoint: Day 0 Day 8 Day 15 Day 30

Secondary

MeasureTime frame
serum uric acidTimepoint: Day 0 Day 30

Countries

India

Contacts

Public ContactDr Jeevan Sampat Jadhav

Shree Saptashrungi Ayurved Mahavidyalay and Hospital ,Nashik

ravindrasphadol@gmail.com9975641619

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026