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This study is to know how Guduchi Churna and Dhatrayadi Kwatha work in raised uric acid

A Randomised Controlled Clinical Study to evaluate the efficacy of Guduchi Churna and Dhatrayadi Kwatha in the management of Vatarakta with special reference to Hyperuricemia - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101710
Enrollment
30
Registered
2026-01-21
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: M205- Other deformities of toe(s) (acquired)

Interventions

None listed

Sponsors

RAJIV GANDHI GOVERNMENT POST GRADUATION COLLEGE AND HOSPITAL PAPROLA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patient of either gender in the age group between 30 to 60 years. 2 Patients having serum uric acid level more than 7 mg per dl in male and more than 6 mg per dl in female with or without any associated features of joint inflammation. 3 Willing to participate and able to provide signed informed consent.

Exclusion criteria

Exclusion criteria: 1 Patients not willing for the trial. 2 Patient suffering from any other form of arthritis like osteoarthritis, tubercular arthritis, rheumatoid arthritis etc. 3 Patients suffering from uncontrolled diabetes, chronic renal diseases, respiratory illness, serious cardiac and hepatic disorders. 4 Patients having any active malignancy. 5 Patients who have completed participation in any other clinical trial during the past 3 months. 6 Any condition which the principal investigator thinks may jeopardize the study.

Design outcomes

Primary

MeasureTime frame
To evaluate the efficacy of Guduchi Churna and Dhatrayadi Kwatha in the management of Vatarakta w.s.r. to Hyperuricemia.Timepoint: 60 days

Secondary

MeasureTime frame
To compare the efficacy of Guduchi Churna and Dhatrayadi Kwatha with Febuxostat in the management of Vatarakta w.s.r. to Hyperuricemia. To assess the clinical safety of Guduchi Churna and Dhatrayadi Kwatha in the management of Vatarakta w.s.r. to Hyperuricemia. Timepoint: 60 days

Countries

India

Contacts

Public ContactDr Anjali Sharma

RAJIV GANDHI GOVT PG AYURVEDIC COLLEGE AND HOSPITAL PAPROLA

drazimal3@gmail.com9418082636

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026