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Patoladi Ghana Vati in the Care of Gout

Randomized controlled clinical trial to determine the efficacy of Patoladi Ghana Vati in the Management of Vatarakta w.s.r. to Gout. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110845
Enrollment
34
Registered
2026-05-21
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: M00-M99- Diseases of the musculoskeletal system and connective tissue

Interventions

None listed

Sponsors

Department of kayachikitsa SSTAC Sangamner Ahmednagar Maharashtra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)patient whose informed written consent has been taken. 2)Patients with classical signs and symptoms of Vatarakta (Sandhishul, Daha, Sandhishotha, Sparshasahatva, Walking impairment ) will be included. 3)Irrespective of gender & socioeconomic condition. 4)Age 18 to 60 Years. 5)Patient with Hyperuricemia above 7 mg/dl with Symptoms of gout.

Exclusion criteria

Exclusion criteria: 1)K/C/O with metabolic disorders and other systemic disease. 2)K/C/O with autoimmune disease of joints. 3)Known patient who are on regular NSAIDS like naproxen, indomethacin. and Steroidal Anti-inflammatory drug. 4)Pregnancy and Lactating mother.

Design outcomes

Primary

MeasureTime frame
1. Change in Sandhishula, Daha, Sandhishotha, Sparshasahatva, and walking ability from baseline to 28 days. 2. Change in serum uric acid levels before and after treatment. Timepoint: 28 days.

Secondary

MeasureTime frame
1.Overall clinical improvement based on percentage relief criteria. 2. Comparative statistical analysis between and within study groups. Timepoint: 28 days

Countries

India

Contacts

Public ContactDr Nilesh Dere

SSTAC Sangamner

dr.nilesh.dere@gmail.com9271292389

Outcome results

None listed

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