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Paliperidone ER Versus Risperidone for Neurocognitive Function in Patients With Schizophrenia: a Randomized, Open-label, Controlled Trial
Primary objective: To examine whether the switch to paliperidone ER from risperidone improves cognitive function in stabilized patients with schizophrenia. Secondary objectives: To compare the general clinical outcomes (efficacy and safety) after switching to paliperidone ER from risperidone
This is a 12-week, randomized, parallel-group, open labeled, flexible-dose study. The patients will be randomized to the risperidone-continuation group in which they continue to receive risperidone, or to the paliperidone-switch group in which they are switched from risperidone to paliperidone. In the paliperidone-switch group, risperidone will be tapered off during the first 4 weeks of the study, while paliperidone is titrated simultaneously. The doses of both drugs will be adjusted according to the clinical judgment of each research psychiatrist, within 6 mg/day of risperidone and 12 mg/day of paliperidone.
Age
18 - 59 years
Sex
ALL
Healthy Volunteers
No
Dept. of Psychiatry, Chonnam National Univeristy Hospital
Gwangju, South Korea
Start Date
November 1, 2008
Primary Completion Date
February 1, 2011
Completion Date
February 1, 2011
Last Updated
December 23, 2011
58
ACTUAL participants
Paliperidone ER
DRUG
Risperidone
DRUG
Lead Sponsor
Chonnam National University Hospital
Collaborators
NCT07455929
NCT06740383
Data Source & Attribution
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