Schizophrenia Clinical Trial
Official title:
Multicenter, Single Group Study of Aripiprazole Efficacy and Safety in the Acute Psychosis Treatment of Schizophrenia, Schizophreniform Disorder and Schizoaffective Disorder.
The purpose of this study is to prove safety and efficacy of aripiprazole.
This study was designed to prove safety and efficacy of aripiprazole in the treatment of
acutely relapsed patients with diagnoses of schizophrenia or schizoaffective disorder in
Korea and to confirm the maintenance of efficacy and safety during maintenance period and
the changes in emotional factors and social functions.
After administering 15 mg/day of aripiprazole for two weeks, the test may change the dose
within the range of 10 mg and 30 mg per day by clinical judgment. (Medication duration: 8
weeks (acute phase) + 18 weeks (maintenance phase)] + 26 weeks (extension phase), *total 52
weeks)
;
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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