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Effect of Unani drugs in gout

Efficacy of Habb-e-Chobchini (Oral administration) and Dimad Muhallil (topical application) in Niqris (Gout)(NUMC: L-7; ICD: M10): A randomised single blind double dummy placebo controlled clinical trial - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094505
Enrollment
87
Registered
2025-09-10
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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: Habb-e-Chobchini and Dimad Muhallil: Habb-e-Chobchini orally 500mg twice daily for 56 days and Dimad Muhallil topically once in a day for 56 days Control Intervention1: Placebo Dimad a

Sponsors

Central Council for Research in Unani Medicine New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged between 18-65 years of any gender Patients with uric acid level more than 7 mg/dl and less than 9.5 mg/dl Patients having capacity and willingness to give consent and complete trial documentation

Exclusion criteria

Exclusion criteria: Patients below 18 years and above 65 years Patients who are known cases of Renal, Cardiac, Liver and Pulmonary diseases Pregnant and Lactating females Patient with uncontrolled Hypertension (SBP more than 140 mm Hg, DBP more than 90 mm Hg) Patients with uncontrolled Diabetes Mellitus (RBS more than the normal range, in patients on Insulin therapy

Design outcomes

Primary

MeasureTime frame
serum uric acidTimepoint: 56 days

Secondary

MeasureTime frame
Improvement in subjective parameters along with improvement in Quality of life Reduction in CRP and ESR level from baseline to the end of the treatmentTimepoint: 56 days

Countries

India

Contacts

Public ContactFarooqui Shazia Parveen Barkat Ali

Regional Research Institute of Unani Medicine Chennai

shaziafarooquinium@gmail.com08147438868

Outcome results

None listed

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