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Treatment of Malarial Fever by Unani medicine Malerian

Clinical Validation of Unani Pharmacopoeial Formulation Malerian in ḤummÄ? AjÄ?miyya (Malarial Fever)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/05/025253
Enrollment
30
Registered
2020-05-20
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: B529- Plasmodium malariae malaria without complication

Interventions

Intervention1: Malerian: 6ml orally twice daily with water for 2 weeks Control Intervention1: Nil: Nil

Sponsors

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

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either sex of age 18-65 years. 2. Presence of axillary temperature >= 37.5°C (99.5 o F) or oral temperature of > 38 o C (100.4 o F) or history of fever during the past 24 hours. 3. Mono-infection with P. vivax confirmed by either positive blood smear (i.e. no mixed infection) or RDT (Rapid Diagnostic Test).

Exclusion criteria

Exclusion criteria: 1. Any evidence of severe malaria that would require hospitalization for treatment i.e. including: impaired consciousness, respiratory distress, severe anaemia (Hb hypotension abnormal bleeding or hypoglycaemia. (acc. to WHO definition) 2. Mixed or mono-infection with Plasmodium species other than P. vivax detected by microscopy. 3. Patients associated with other known conditions requiring long term treatment like TB, AIDS, diabetes, hypertension etc. 4. Reported allergy to any antimalarial drugs, including sulfa and artemisinin drugs. 5. Patients with Glucose-6-phosphate dehydrogenase deficiency 6. Pregnant and lactating females.

Design outcomes

Primary

MeasureTime frame
Improvement in signs and symptoms of ḤummÄ? AjÄ?miyya (Malarial Fever)Timepoint: 2 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 (CCRUM)

ccrum507@rediffmail.com9213511298

Outcome results

None listed

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