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Study the effect of decoction of pippal bark and Guduchi in pain and swelling in leg joints

Comparative phase 2 clinical study to evaluate efficacy of Ashvattha twak kashay and Guduchi kashay in Vatarakta with special reference to Gout

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/09/027991
Enrollment
60
Registered
2020-09-23
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: M859- Disorder of bone density and structure, unspecified

Interventions

Intervention1: Ashvattha Twak Kashay: 40 ml twice daily before meal with water for 30 Days Control Intervention1: Guduchi Kashay: 40 ml twice daily with water for 30 days

Sponsors

Ayurved Mahavidyalaya Nashik
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients diagnosed as Vatarakta with classical symptoms according to Acharya Charaka such as Sandhishula Sandhidaha Sandhi sparshasahatva sandhishoth sandhivaivarnya Patient with Serum Uric Acid Level > 7.0mg/dl in Males and >5.7 in females Patient willing for trial and giving written consent Patient with all socio-economic status

Exclusion criteria

Exclusion criteria: Patients with known case of major systemic disorder such as MI Uncontrolled DM Uncontrolled Hypertension Renal disease Hepatic disease etc Patients having arthritis other than Gouty Arthritis Complicated cases of Vatarakta by its upadravas like Hikka Murchha Moha Visarpa Mans-Koth etc Pregnant and Lactating women

Design outcomes

Primary

MeasureTime frame
Reduction in signs and symptoms of VataraktaTimepoint: 30 Days

Secondary

MeasureTime frame
Reduction in uric acid levelTimepoint: 30 days

Countries

India

Contacts

Public ContactDr Eknath G Kulkarni

Ayurved Seva Sangh Ayurved Mahavidyalaya Nashik Maharashtra

ekulkarni6@gmail.com8263941291

Outcome results

None listed

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