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Study of the effect of Atomoxetine on cognitive symptoms in patients with schizophrenia

Phase 2
Recruiting
Conditions
schizophrenia.
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F00-F98
Registration Number
IRCT20101130005280N31
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
42
Inclusion Criteria

2nd Generation Antipsychotic Drug use
Lack of dementia
Not taking other medicines (except anticholinergics and benzodiazepines)
No pregnancy or breastfeeding
There is no recent history of drugs (except nicotine)
schizophrenic patients during partial recovery

Exclusion Criteria

Drug side effects including: abdominal discomfort, loss of appetite resulting in weight loss, dizziness, irritability and mood swings
Occurrence of drug interactions with patient medications

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cognitive function. Timepoint: Before intervention, end of first and second. Method of measurement: PANSS?Wisconsin? Stroop? Digit Span Questionier.
Secondary Outcome Measures
NameTimeMethod
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