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Effect of Unani medicine Khamira Gawzaban Sada in Zuâ??f al-DimÄ?gh (Cerebro-asthenia)

Clinical Validation of a Unani Pharmacopoeial formulation â?? Khamira Gawzaban Sada in Zuâ??f al-DimÄ?gh (Cerebro-asthenia)

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/09/015692
Enrollment
300
Registered
2018-09-11
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: G31- Other degenerative diseases of nervous system, not elsewhere classified Health Condition 2: null- Zuâ??f al-DimÄ?gh (Cerebro-asthenia)

Interventions

Intervention1: Khamira Gawzaban Sada: 10 grams orally once daily to be taken with water before breakfast for six weeks Control Intervention1: nil: nil

Sponsors

Central Council for Research in Unani Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The patients fulfilling the following criteria will be included in this study: 1. Patients of any sex in the age group 19-70 years 2. Patients of Zuâ??f al-DimÄ?gh (Cerebro-asthenia) having: ï?§ Subjective complaints of cognitive impairment ï?§ 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. Patients with impairment of speech, hearing and vision, which can impede the interview for MMSE and QOL assessment 3. Known cases of hypothyroidism or hyperthyroidism 4. Vitamin B12 deficiency 5. Patients on Psychotropic Drugs 6. Clinical presentation and/or history of a chronic disease that requires long-term treatment, e.g., DM, tuberculosis, HIV infection, syphilis, CVD, pulmonary disease, CKD, chronic liver disease, or any other serious and/or unstable medical condition that, in the opinion of the investigator, could expose the patients to undue risk of a significant adverse event or interfere with assessment of safety or efficacy during the course of the trial 7. Pregnant and lactating women 8. H/o Addiction (alcohol, drugs) 9. H/o Hypersensitivity to the study drug or any of its ingredients

Design outcomes

Primary

MeasureTime frame
Improvement in signs and symptoms of Zuâ??f al-DimÄ?gh (Cerebro-asthenia) Timepoint: 6 weeks

Secondary

MeasureTime frame
Haematological and biochemical assessment for safety assessmentTimepoint: at baseline and at the end of treatment

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine

ccrum507@rediffmail.com

Outcome results

None listed

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