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Efficacy and Safety of a Unani Formulation in the management of Gouty Arthritis

A Clinical Study to Evaluate the Efficacy and Safety of a Unani Formulation in the management of Niqris(Gouty Arthritis) : A Randomized Controlled Clinical Trial. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072426
Enrollment
66
Registered
2024-08-13
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: Polyherbal unani formulation of, Suranjan sheerin(colchicum luteum),3.5 gram Zanjabeel khushk(zinjiber officinalis), 3.5 gram Sibr(aloe barbadensis), 7 gram: Dosage form: Safuf (powder)
Suranjan sheerin(colchicum luteum),3.5 gram Zanjabeel khushk(zinjiber officinalis), 3.5 gram Sibr(aloe barbadensis), 7 gram Control Intervention1: Febuxostat: Febuxostat, Dosage form: Tablet, Dose:

Sponsors

FARHA LUQMAN
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Clinically diagnosed patient of Gout with raised Serum uric acid level beyond normal limit Both sexes Clinically stable Patient

Exclusion criteria

Exclusion criteria: Patient below 20 and above 65 years. Gout with Diabetic Mellitus. Pregnant women and lactating mother. Severe illnesses of debilitated patients of cardiovascular system ,respiratory system, severe renal or hepatic insufficiency, gastro- intestinal problems, nervous system and malignant growth. Any other type of arthritis such as Rheumatoid Arthritis, Osteoarthritis etc.

Design outcomes

Primary

MeasureTime frame
Response to treatment will be assessed using the following parameter 1-Reduction in uric acid 2-Reduction in C. Reaction 3-Improvement in Patients Global Assessement (PGA) based on VASTimepoint: 2week 4 week 6 week 8 week

Secondary

MeasureTime frame
Adverse effect kidney function test liver function test haemoglobinTimepoint: 8 week

Countries

India

Contacts

Public ContactDr Mohd Zubair

Stat,e Takmeel-ut-Tib College and Hospital

mzaligmd@gmail.com8318016554

Outcome results

None listed

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