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Treatment of Fever with Unani medicine Cap Mubarak

A Single-blind, Randomized, Parallel group study to evaluate antipyretic effect of Unani Medicine formulation– Cap Mubarak compared to controlled drug Tab Paracetamol in patients with Humma (fever) - Not applicable

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061859
Enrollment
60
Registered
2024-01-25
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: R509- Fever, unspecified

Interventions

Intervention1: Cap Mubarak: 2 Cap of 500 mg to be taken orally twice daily with water for 3 days Control Intervention1: Tab Paracetamol: 1 Tab of 500 mg to be taken orally twice daily with water for

Sponsors

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

Eligibility

Inclusion criteria

Inclusion criteria: 1. Participants of either sex in the age group 18 to 65 years. 2. History of onset of fever within 24 hr. 3. Participants with oral temperature 100 F- 102 F presenting with any of the following symptoms: Fever Headache Body ache Joints pain Shivering Chills Palpitation Skin Flushing

Exclusion criteria

Exclusion criteria: 1. Intake of any antipyretic drugs in the previous 8 hrs. 2. Participant having oral temperature of greater than 102 F. 3. Known high risk clinical conditions such as pneumonia, sepsis, dengue haemorrhagic fever,meningitis, hepatitis B, etc. 4. Known cases of Immuno-compromised clinical conditions such as HIV, cancer etc. 5. Known cases of other clinically significant co-morbid conditions (severe hepatic, renal, cardiovascular disorders, etc.) that in the opinion of the investigator could affect the efficacy and safety outcome of the study. 6. Thrombocytopenia i.e. absolute platelet count below 1,00,000. 7. Known hypersensitivity to study drug or any of its ingredients. 8. Pregnant and Lactating females. 9. Diabetes Mellitus or any systemic disorder requiring prolonged treatment.

Design outcomes

Primary

MeasureTime frame
The efficacy of the study drug in the treatment of Humma (fever) will be assessed on the basis of reduction in the symptoms and change in temperature from baseline to end of the study and the achievement of defervescence,Timepoint: At baseline and on 3rd day

Secondary

MeasureTime frame
Haematological & biochemical assessment for safety assessment i.e. CBC, LFT, KFT, Urine Routine & microscopic examination.Timepoint: At baseline and end of treatment i.e. 3rd day.

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine (CCRUM)

naheedparveen802@gmail.com9213511298

Outcome results

None listed

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