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An investigation on the effect of memantine on children with autistic spectrum disorder

Not Applicable
Conditions
patients diagnosed with ASD.
Autistic disorder
F84.0
Registration Number
IRCT20211118053097N1
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
52
Inclusion Criteria

Patients diagnosed with ASD according to DSM 5
Patients with no previous history of epilepsy and/or abnormal electroencephalography
Patients aged between 4 to 12 years old

Exclusion Criteria

Intolerance to Memantine
Patients and/or their caregiver’s disinclination to continuing with trail

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Electroencephalography analysis. Timepoint: Before the treatment and 10 weeks after treatment onset. Method of measurement: Using the Electroencephalograph and analysis of activities.;ABC questionnaire (measuring cognitive activity). Timepoint: Before the treatment and 10 weeks after treatment onset. Method of measurement: Filling ABC autism questionnaire.
Secondary Outcome Measures
NameTimeMethod
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