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Effect of supplementation in treatment of schizophrenia patients

Phase 2
Conditions
Schizophrenia.
Schizophrenia
Registration Number
IRCT2017072333551N2
Lead Sponsor
Vice chancellor for research, Kashan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Diagnosed with schizophrenia using DSM-IV-TR criteria
PANSS score of 55 or greater
Treated with chlorpromazine (300–1000mg/day, except clozapine) and agents anti-cholinergic (Trihexyphenidyl, 4–8 mg/day) during the last 6 months
Aged 25–65 years old
Disease duration of at least two years

Exclusion Criteria

Mental retardation
Substance or alcohol addiction (except caffeine or nicotine) with in the last 6 months of screening
A score of=14 on a 17-item Hamilton Depression Rating Scale or a score of =4 on PANSS (depression item)
Under treatment with lithium, carbamazepine and sodium valproic acid
Existing chronic and acute medical illness
Lactation or pregnancy
The use of anti-depressants including MAO, TCA, SSRI in the last 6 months

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Positive and Negative Syndrome Scale(PANSS). Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: Clinical Examination.
Secondary Outcome Measures
NameTimeMethod
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