NCT00292409
Completed
Phase 3
A Prospective Open-Label Study of Aripiprazole in the Management of Patients With Schizophrenia in General Psychiatric Practices
DrugsAripiprazole
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Schizophrenia and Schizoaffective Disorder
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc.
- Enrollment
- 400
- Primary Endpoint
- Clinical Global Impression-Improvement at endpoint
- Status
- Completed
- Last Updated
- 12 years ago
Overview
Brief Summary
The purpose of this clinical research study is to evaluate the overall effectiveness of 8 week of aripiprazole treatment.
Investigators
Eligibility Criteria
Inclusion Criteria
- •diagnosis of schizophrenia or schizoaffective disorder being treated as outpatients,no response to past antipsychotic treatment and patients who symptoms are notoptimally controlled defined as CGI- S\<7
Exclusion Criteria
- •pregnant or breastfeeding,patients at risk for committing suicide,diagnosis of mood disorders, delirium, dementia and other cognitive disorders,patients treatment resistant to otherantipyschotic medications and treatment with a long acting psychotic in which the last dose was within 3 months of treatment phase
Outcomes
Primary Outcomes
Clinical Global Impression-Improvement at endpoint
Secondary Outcomes
- Investigator's Assessment Questionnaire
- Patient preference of medication at endpoint
- Clinical Global Impression scale
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