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A Study on Gout to evaluate the safety and efficacy of Polyherbal formultion.

A single blind observational study to evaluate the safety and efficacy of polyherbal formulation in the management of Niqris (Gout). - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072000
Enrollment
30
Registered
2024-08-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Intervention1: Drugs namely Suranjan (ColchicumLuteum), Khulanjan (Alpinia Galanga) and Bozidan (Pyrethrum Indicum): The drugs will be ground into fine powder then 5 grams of the drug will be given th

Sponsors

Islamic University of Science and Technology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients of either sex will be selected for the study. 2.Between 18 to 60 years of age. 3.Fulfilling the criteria of American College of Rheumatology for diagnosing Gouty Arthritis including clinical features, laboratory, and radiological finding will be included in the study, who had serum Uric Acid level more than 7mg/dl.

Exclusion criteria

Exclusion criteria: 1.Patients below 18 and above 60 years of age. 2.Pregnant and Lactating mothers. 3.Patients who fail to give consent. 4.Patients of Gout associated with any systemic disorder which interfere with patient study will be excluded. 5.Patients of Gout associated with any severe Arthritis condition. Such as Rheumatoid arthritis, Septic arthritis will be excluded from the study 6.Patients suffering from Anemia and other blood dyscrasias like leukemia, hemophilia etc 7.Patients with history of suffering with congenital Gout.

Design outcomes

Primary

MeasureTime frame
1.Serum uric acid level. 2.CRP 3.ESR Timepoint: 2 years

Secondary

MeasureTime frame
1 Pain Tenderness and Swelling in the affected joints 2 Difficulty in movement. 3 Affected joint redness (Erythema). Timepoint: 2 years

Countries

India

Contacts

Public ContactDr Tabasum Fatima

Islamic University of Science and Technology

tabasumfatima281@gmail.com9419421375

Outcome results

None listed

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