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Ayurvedic management of vata rakta(Gout) by Siravedhana and Mustadi Yapana Basti

A Randomized Comparative Clinical Study Evaluating the Efficacy of siravedhana followed by Modified Bala Guduchyadi Yapana Basti and Mustadi Yapana Basti in the Management of Vatarakta wsr to Gout - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088989
Enrollment
20
Registered
2025-06-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: M109- Gout, unspecified

Interventions

None listed

Sponsors

Parul Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects presenting with classical clinical features of Vatarakta. 2. Subjects of either gender between age group of 18-70 yr. 3. Subjects fit for Niruha and Anuvasna basti karma. 4. Uric Acid level ABove 6 mg /dl in female. 5. Uric acid level ABove 7 mg/dl in male.

Exclusion criteria

Exclusion criteria: 1. Subjects with chronic autoimmune disease of joints & with joint deformity due to it 2. Subjects with uncontrolled metabolic systemic disorder like HTN and DM 3. Pregnant and lactating women. 4. Subjects contraindicated for Niruha and Anuvasana Basti. 5. Subjects with Alpa bala.

Design outcomes

Primary

MeasureTime frame
Reduction in symptoms of VataraktaTimepoint: 4th day of treatment- first follow up and assesment of parameters 20th day of treatment- second follow up and assesment of parameters

Secondary

MeasureTime frame
Reduction in uric acid levelsTimepoint: 4th day of treatment- first follow up & assesment of parameters 20th day of treatment- second follow up & assessment of parameters

Countries

India

Contacts

Public ContactDr Sangeeta H Toshikhane

Parul institute of ayurved

sangeeta.toshikhane26791@paruluniversity.ac.in9964596479

Outcome results

None listed

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