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

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Otsuka

Status

Completed

Conditions

Schizophrenia
Bipolar Disorder

Treatments

Drug: Aripiprazole

Study type

Observational

Funder types

Industry

Identifiers

NCT00216723
Korea Abilify PMS

Details and patient eligibility

About

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

Full 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.

Enrollment

3,000 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

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)

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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