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Treatment of weakness of brain and memory (Zof-e-Dimag wa Hafiza) with Unani drugs Majoon Brahmi and Majoon e Nisyan

Comparative Clinical Validation study of Unani Pharmacopoeial Formulation Majoon Brahmi vs Majoon e Nisyan in Zof-e-Dimag wa Hafiza (Cerebro-asthenia) - NILL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092256
Enrollment
110
Registered
2025-08-04
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: F488- Other specified nonpsychotic mental disorders

Interventions

Intervention1: Majoon Brahmi: 5 gm BD with water for 6 weeks. Control Intervention1: Majoon e Nisyan: 5 gm BD with water for 6 weeks.

Sponsors

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

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of Zof-e-Dimag wa Hafiza (Cerebro-asthenia) having subjective complaints of cognitive impairment: . Memory loss . Mild headache . speech impairment . writing impairment 2. MMSE score of 10-23 representing mild to moderate cognitive impairment.

Exclusion criteria

Exclusion criteria: 1. Clinical presentation and/or history of any significant organic neurological diseases including space occupying lesions, stroke, head injury, seizure, and mental retardation. 2. Secondary causes of dementia including hypothyroidism or hyperthyroidism. 3. Known cases of B12 vitamin deficiencies. 4. Known case of chronic diseases that requires long-term treatment. 5. Patients on Psychotropic Drugs 6. H/o alcohol or substance abuse or dependence. 7. H/o Hypersensitivity to the study drug or any of its ingredients. 8. Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
The safety and efficacy of Unani Pharmacopeial formulation Majoon Brahmi in comparison with Majoon e Nisyan in Zof-e-Dimag wa Hafiza (Cerebro-asthenia) will be carried out on the basis of Mini Mental State Examination (MMSE) scoreTimepoint: At Baseline and after every 14 days, (i.e., 0, 14th,28th and 42th day)

Secondary

MeasureTime frame
Haematological & biochemical assessment for safety assessment i.e. CBC, LFT, KFT, Urine Routine & microscopic examination.Timepoint: At baseline, at first follow up and at the end of treatment. (i.e., At 0, 14th and 42th day)

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine (CCRUM)

javed.ghazal@gmail.com09811810454

Outcome results

None listed

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