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Evaluation of the effectiveness of Boswellia -based herbal powder mixture in improving of Alzheimer's patients

Phase 3
Recruiting
Conditions
Mild to moderate Alzheimer's.
Alzheimer's disease
Registration Number
IRCT20210701051755N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
64
Inclusion Criteria

people over 50 years old
who have been diagnosed with mild to moderate Alzheimer's disease based on a clinical interview with a DSM-V neurologist
Minimum primary education

Exclusion Criteria

Major psychiatric disorders such as depression, schizophrenia; psychotic disorders
Other causes of dementia include pure vascular dementia, airway dementia, and frontotemporal dementia.
Treatable causes of dementia such as metabolic disorders
Patients with severe hepatic impairment (Child-Pugh class c), renal (GFR <25 ml / min) and cardiac (EF <15%)
Taking the drug memantine
Taking any medication or herbal supplement with an effect on cognitive function
Reluctance to continue the plan, at any time and for any reason during the study
Serious side effects during treatment

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Score of cognitive disorders in MMSE, MOCA questionnaires. Timepoint: 3 months from the start of the study. Method of measurement: MMSE(Mini–mental state examination), MOCA(montreal cognitive assessment).;Behavioral Disorders Score in NPI Questionnaire. Timepoint: 3 months from the start of the study. Method of measurement: (Neuropsychiatric Inventor)NPI test.
Secondary Outcome Measures
NameTimeMethod
Investigation of side effects. Timepoint: monthly. Method of measurement: Ask questions of the patient and record information.
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