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Effect of Boozidaan(Pyrethrum Indicum)on Niqris Muzmin(chronic gout)

Clinical study to Evaluate Safety And Efficacy of Bozidan(Pyrethrum Indicum) in the management of Niqris Muzmin (Chronic Gout).

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/03/032150
Enrollment
60
Registered
2021-03-19
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: M1A9- Chronic gout, unspecified

Interventions

Intervention1: safoof(powder) of unani formulation: Ingredient:Boozidan(Pyrethrum Indicum)5gm orally in the form of safoof once daily after breakfast with water for 28 days Control Intervention1: Febu

Sponsors

Central council for Research in Unani Medicine New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Irrespective of all genders Patients between 18-65 years of age Patients Fulfilling the criteria of American College of Rheumatology(ACR) for diagnosing gouty arthritis including clinical features, laboratory and radiological finding , having serum uric acid level >7mg/dl in males and Ë?6mg/dl in females17. Patients, who are ready to sign the informed consent, follow the protocol and willing to participate in clinical study voluntarily

Exclusion criteria

Exclusion criteria: Patients below 18 and above 65 years of age Pregnant and lactating mothers Patients who fail to give consent Patients of gout associated with any systemic disorder which interfere with patient study Patients of gout associated with any severe arthritic condition such as rheumatoid arthritis, septic arthritis. Patients suffering from anemia and other blood dyscrasias like leukemia, haemophilia,etc Patients suffering from congenital gout Any other disease other than Gout(Gouty arthritis).

Design outcomes

Primary

MeasureTime frame
Relief in Signs and Symptoms of Chronic gout and normal Uric acid levelsTimepoint: 28 days

Secondary

MeasureTime frame
Haematological and biochemical assessment for safetyTimepoint: 28 days

Countries

India

Contacts

Public ContactDr Towseef Amin Rafeeqi

Regional Research Institute of Unani Medicine

naquibislam@yahoo.co.in9469154930

Outcome results

None listed

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