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Treatment of Cerebro-asthenia by Unani medicine Habbe Jadwar Kochak

Clinical Validation of Unani Pharmacopoeial Formulation Habb e Jadwar Kochak in á¸?uâ??f al-DimÄ?gh (Cerebro-asthenia)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/07/026544
Enrollment
300
Registered
2020-07-14
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: F488- Other specified nonpsychotic mental disorders

Interventions

Intervention1: Habbe Jadwar Kochak: 125 mg Orally twice daily to be taken with water for 6 weeks Control Intervention1: Nil: Nil

Sponsors

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

Eligibility

Inclusion criteria

Inclusion criteria: The patients fulfilling the following criteria will be included in this study: 1. Patients of either sex in the age group 40-65 years. 2. Patients of á¸?uâ??f al-DimÄ?gh (Cerebro-asthenia) having subjective complaints of cognitive impairment: a. Memory loss b. Mild headache c. Anxiety d. ButlÄ?n-i-Takallum (Speech impairment) e. ButlÄ?n-i-TahrÄ«r (Writing impairment) 3. MMSE score of 10-23 representing mild to moderate cognitive impairment

Exclusion criteria

Exclusion criteria: The patients having any of the following criteria will be excluded from the study: 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. Clinical presentation and known case of a chronic disease 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
Improvement in sign and symptoms of á¸?uâ??f al-DimÄ?gh (Cerebro-asthenia)Timepoint: 6 Weeks

Secondary

MeasureTime frame
Haematological and biochemical assessment for safety assessmentTimepoint: Investigations will be done at baseline and after every two weeks

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