A Study to Understand Gout(Vatarakta) and the Effect of Guduchi and Patol Patra Churna

An Aetiopathological Study of Vatarakta with special reference to Gout and A Comparative Study of Guduchi and Patol Patra Churna - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/01/100073

Enrollment

Registered

2026-01-01

Start date

Unknown

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

Health Condition 1: E70-E88- Metabolic disorders

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. The patients having age between 20 to 60 years of either sex. 2. The patient sign and symptoms should be based on ayurvedic view. 3. The patients willing for trial.

Exclusion criteria

Exclusion criteria: 1. Age above 60 and less than 20 years. 2. Immunocompromised patients e.g. HIV etc. 3. Severe deformities. 4. Pregnant and lactating women.

Design outcomes

Primary

Measure	Time frame
Determination of the effect of the intervention with respect to other 1. Sandhi Ruk (Pain in affected joint) 2. Sandhi Shotha (Swelling in affected joint) 3. Daha (Burning sensation) 4. Sandhi Toda (Pricking sensation in joints) 5. Twak Vaivarnya (Discoloration of skin) 6. Kandu (Itching) Timepoint: The assessment of patients will be conducted at 15-day intervals during treatment. Duration- 60 Days	—

Measure

Time frame

Determination of the effect of the intervention with respect to other 1. Sandhi Ruk (Pain in affected joint) 2. Sandhi Shotha (Swelling in affected joint) 3. Daha (Burning sensation) 4. Sandhi Toda (Pricking sensation in joints) 5. Twak Vaivarnya (Discoloration of skin) 6. Kandu (Itching) Timepoint: The assessment of patients will be conducted at 15-day intervals during treatment. Duration- 60 Days

—

Secondary

Measure	Time frame
Change in Serum Uric Acid Level from before treatment to the end of treatmentTimepoint: The assessment of patients will be conducted at 15-day intervals during treatment.	—

Countries

India

Contacts

Public ContactDr Basant Kumar Thakur

Government Ayurvedic College and Hospital, Kadamkuan, Patna

drbkthakur@rediffmail.com7004568326

Outcome results