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The effect of Palmitoylethanolamide on the treatment of negative symptoms in patients with chronic schizophrenia

Phase 2
Conditions
Schizophrenia.
Schizophrenia
Registration Number
IRCT20090117001556N127
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
50
Inclusion Criteria

Age between 18 to 60 years
Take Risperidone for at least 4 weeks at the dose of 4-6 mg/day before entering the study
The positive and acute symptoms of patients should be stable

Exclusion Criteria

Head trauma
History of shock therapy during past three months prior to the trial
Undergoing neurosurgery
Presence of acute or chronic systemic diseases
History of allergy to Cilostazol

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of schizophrenia. Timepoint: Baseline and weeks 4 and 8. Method of measurement: By Positive and Negative Syndrome Scale (PANSS).
Secondary Outcome Measures
NameTimeMethod
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