The purpose of this study is the evaluation of effectiveness of paliperidone palmitate within three different group of schizophrenia patients.
In this study, the investigators are going to examine the effectiveness of paliperidone palmitate after changing from other antipsychotics. This study design is a Prospective Naturalistic Case Series Study. The effectiveness of paliperidone would be compared within three different groups of schizophrenia. Investigators would also assess the safety during 24 weeks follow up period.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
paliperidone palmitate 150mgeq(1 day), 100mgeq(8days), 75mg(monthly)
Seoul National University Hospital
Seoul, South Korea
CGI-S,I: Clinical Global Impression-Severity, Improvement
Time frame: 24 weeks
PANSS: Positive and Negative Syndrome Scale
Time frame: 24 weeks
CRS: Clinician Rating Scale
Time frame: 24 weeks
KDAI-10: Korean Drug Attitude Inventory-10
Time frame: 24 weeks
SWN: Subjective Well-being Under Neuroleptic Treatment
Time frame: 24 weeks
DIEPSS: Drug-Induced ExtraPyramidal Symptoms Sclae
Time frame: 24 weeks
injection site pain -VAS: Visual Analog Scale
Time frame: 24 weeks
LUNSERS: Liverpool University Neuroleptic Side Effect Rating Scale
Time frame: 24 weeks
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