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Treatment of patients suffering with chronic gout with Unani Medicine Habb-e-Leemun

Clinical Validation Study of Unani Pharmacopoeial Formulation Habb -e- Leemun in Niqris (Chronic Gout) - NILL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092459
Enrollment
210
Registered
2025-08-05
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: M1A- Chronic gout

Interventions

Intervention1: Habb-e-Leemun : One tablet Taken orally twice a day after meals with water for 6 weeks. Control Intervention1: NIL: NIL

Sponsors

Central Council for Research in Unani Medicine CCRUM New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Conformed diagnosis of gout meeting ACR criteria (American College of Rheumatology Criteria) for gout. 2. History of recurrent gout flares (more than 2 per year). 3. Persistent symptoms such as joint pain, swelling, or tophi (visible urate deposits) present for at least six months. 4. Chronic hyperuricemia (serum uric acid equal or more than 6.8).

Exclusion criteria

Exclusion criteria: 1. Known cases of joints diseases (Osteoarthritis, Osteomyelitis, Rheumatoid Arthritis) except Gout. 2. Patients with systemic diseases like Diabetes Mellitus, Hypertension, and Cardiovascular diseases. 3. Grade-2 obesity (BMI more than 35). 4. Hepatic and renal insufficiency and any malignancy. 5. Patient on long term medication. 6. Patients on drugs that increase uric acid levels. (Thiazide diuretics) or decrease calcium levels (furosemide). 7. Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
The efficacy of the Habb -e- Leemun in the treatment of Niqris (Chronic Gout) will be carried out on the basis of Pain (VAS-Visual Analogue Scale) and Gout Assessment Questionnaire.Timepoint: At baseline, at first follow up and at the end of treatment. i.e., 0, 2nd, 6th weeks

Secondary

MeasureTime frame
Haematological and biochemical investigations for safety assessment i.e., Hemogram, LFT, KFT,Serum Uric acid, HbA1c, CRP and Urine Examination: Routine & Microscopic. Timepoint: At baseline, at first follow up and at the end of treatment. i.e., 0, 2nd, 6th weeks

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine (CCRUM)

drpradeepkumar2001@yahoo.com9811810454

Outcome results

None listed

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