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Clinical Trials/NCT00216723
NCT00216723
Completed
Not Applicable

Efficacy and Safety of Aripiprazole in Patients With Schizophrenia or Bipolar Disorder

Korea Otsuka Pharmaceutical Co., Ltd.2 sites in 1 country3,000 target enrollmentApril 2004

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Schizophrenia
Sponsor
Korea Otsuka Pharmaceutical Co., Ltd.
Enrollment
3000
Locations
2
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

This is a multicenter,open-label,prospective study of Aripiprazole use in patients with schizophrenia and bipolar disorder.

Detailed Description

This is a multicenter,open-label,prospective study of Aripiprazole use in patients with schizophrenia and bipolar disorder. Qualified schizophrenia patients will be enrolled to an 12-week treatment phase of Aripiprazole by physician's assessment. Qualified bipolar disorder patients will be enrolled to an 8-week treatment phase of Aripiprazole by physician's assessment. This study will be continued for 6 years. The final report of Aripiprazole PMS will be submitted to KFDA on December 28, 2009.

Registry
clinicaltrials.gov
Start Date
April 2004
End Date
December 2009
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patient with a schizophrenia or schizoaffective disorder or bipolar disorder according to DSM-IV criteria
  • Age: more than 18 years of age

Exclusion Criteria

  • Unqualified patients judged by study investigator(s)

Outcomes

Primary Outcomes

Not specified

Study Sites (2)

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