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The effect of Atomoxetine on Cognitive Function of Multiple Sclerosis

Phase 3
Recruiting
Conditions
Multiple Sclerosis.
Demyelinating disease of central nervous system, unspecified
G37.9
Registration Number
IRCT20210715051901N1
Lead Sponsor
Ahvaz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
52
Inclusion Criteria

Diagnosis of Multiple Sclerosis based on McDonald's criteria
Age between 18 to 55 years
Testable Measurable Cognitive impairment (MACFIMS) attributed to Multiple Sclerosis

Exclusion Criteria

Continued use of Stimulant
Clinical relapse of Multiple Sclerosis with in 60 days of screening
Changes in the treatment of Multiple Sclerosis within 90 days of screening
Existence of any underlying factor and disease that causes dementia and cognitive impairment
Proof of moderate to severe depression with a Beck's test
Contraindications to the use of Atomoxetine
Confirmation of cognitive impairment related to Multiple Sclerosis with McFimes test

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cognitive Disorder Score in MacFims Questionnaire. Timepoint: Perform MacFims test at the beginning of the study and three months after the start of the study. Method of measurement: MacFims Questionnaire.
Secondary Outcome Measures
NameTimeMethod
Accompanying depression score. Timepoint: At the beginning of the study and 3 months later. Method of measurement: Beck Questionnaire.
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