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Treatment of Severe pain in head with Unani medicine Habb-e-Mujarrrib

Clinical validation of Unani pharmacopeial formulation Habb-e-Mujarrib in Shaqeeqa (Migraine) - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/076028
Enrollment
220
Registered
2024-10-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: G439- Migraine, unspecified

Interventions

Intervention1: Habb-e-Mujarrib: 1 gm pills to be taken orally twice daily with water for 12 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 gender in the age group 18- 65 years 2. Primary diagnosis of Migraine without aura by ICHD-3 beta as follows: A. At least five attacks fulfilling criteria B–D. B. Headache attacks lasting 4-72 hours (untreated or unsuccessfully treated). C. Headache has at least two of the following four characteristics: Unilateral location Pulsating quality Moderate or severe pain intensity Aggravation by or causing avoidance of routine physical activity (e.g. walking or climbing stairs). D. During headache at least one of the following: Nausea and/or vomiting. Photophobia and phono phobia. E. Not better accounted for by another ICHD-3 diagnosis

Exclusion criteria

Exclusion criteria: 1. Known case of any structural brain abnormalities 2. Known case of Ocular disease 3. History of Ischemic stroke 4. Any disease involving sinus e.g. Rhinosinusitis 5. Systemic illness requiring long term treatment 6. Known cases of Chronic kidney & liver disease 7. Known cases of Psychiatric illness 8. Difficulty distinguishing migraine headache from other headaches 9. Known cases of Epilepsy and other neurological disorders 10. History of alcohol and drug abuse. 11. Pregnancy & lactation

Design outcomes

Primary

MeasureTime frame
The efficacy of the study drug will be assessed on the basis of clinical parameters based on grading of symptoms, scoring of MIDAS and any change in rescue medication pattern.Timepoint: At baseline and at every two weeks till the completion of the trial i.e. upto 12 weeks

Secondary

MeasureTime frame
Haematological & biochemical assessment for safety assessment i.e. CBC, LFT, KFT, Urine Routine & microscopic examinationTimepoint: At baseline and at the end of treatment i.e. 12 weeks

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine (CCRUM)

ghazala.javed@gov.in9811810454

Outcome results

None listed

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