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Ayurvedic Management on Memory Impairment

Phase 2
Conditions
Health Condition 1: R298- Other symptoms and signs involvingthe nervous and musculoskeletal systems
Registration Number
CTRI/2019/05/019372
Lead Sponsor
All India Institute of Ayurveda
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients between 41-60 years of age.

Gender: both

Socio-economic status: any

Healthy volunteers willing to participate in the trial and diagnosed to have impaired memory as per the memory scale.

Complaints of memory impairment on the basis of short term and long term.

Short term, e.g. misplacing objects, difficulty in remembering multiple items to be purchased, difficulty in recalling information quickly, problems in remembering names and telephone numbers.

Long term, e.g. difficulty in recall of special events of personal life, difficulty in recall of previous histories of life and recognition.

Mini Mental State Examination.

Hamilton anxiety scale criteria.

Exclusion Criteria

Patients not willing to participate in the clinical trial.

History of any surgical intervention to brain.

Intake of over the counter memory enhancing drugs in the previous 6 months.

Any type of psychosis

Dementia due to brain injury.

Patients with evidence of delirium, confusion or other disturbances of consciousness, Parkinsonâ??s disease, stroke, intracranial haemorrhage, brain tumours, history of alcoholism or drug dependence, use of any psychotropic drug, Alzheimerâ??s disease, diabetes mellitus, endocrinal dysfunction.

Patients with evidence of malignancy.

Patients suffering from major systemic illness necessitating long term drug treatment (Rheumatoid arthritis, Tuberculosis, Psycho-neuro-endocrinal disorders etc)

Patients who have completed participation in any other clinical trial during the past six months.

Any other condition which the Principal Investigator thinks may jeopardize the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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