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Treatment of Gout with Unani medicine Safoof Chobchini

Clinical Validation of Unani Pharmacopoeial Formulation Safoof Chobchini in Niqris (Gout)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/02/017821
Enrollment
240
Registered
2019-02-26
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: M109- Gout, unspecified

Interventions

Intervention1: Safoof Chobchini: 5 gm Orally Twice daily with water after meals Control Intervention1: nil: nil

Sponsors

Central Council for Research in Unani Medicine CCRUM
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: (All of the following) 1. Patients of either sex in the age group of 18-65 years 2. Serum uric acid level: normal or above normal 3. Diagnosed cases of gout as per the ACR/ EULAR-2015 criteria for gout presenting with any of the following symptoms and signs: 4. Joint Pain [especially first metatarsophalangeal (MTP) joint] 5. Tenderness 6. Swelling 7. Redness

Exclusion criteria

Exclusion criteria: (Any of the following) 1. Clinical conditions involving joints e.g. Osteo-arthritis, Rheumatoid arthritis, Rheumatic arthritis 2. Pregnant and lactating women 3. Patients having any systemic diseases such as hypertension, diabetes mellitus, cardiovascular/cerebrovascular diseases, hepatic and renal disease, osteomalacia, osteoporosis 4. Patients with recent H/O dengue, chikungunya and viral fever 5. Grade-2 obesity (BMI >= 35) 6. Patients on long term medications 7. Patients taking drugs which increase serum uric acid levels (thiazide diuretics, etc.) and decrease serum calcium levels (furosemide, etc.)

Design outcomes

Primary

MeasureTime frame
Improvement in sign and symptoms of Niqris (Gout)Timepoint: 6 weeks

Secondary

MeasureTime frame
Haematological and biochemical assessment for safety assessmentTimepoint: Investigations will be done at baseline and end of treatment

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine

ccrum507@rediffmail.com9213511298

Outcome results

None listed

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