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Clinical Trials/NCT00292409
NCT00292409
Completed
Phase 3

A Prospective Open-Label Study of Aripiprazole in the Management of Patients With Schizophrenia in General Psychiatric Practices

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.

Registry
clinicaltrials.gov
Start Date
March 2005
End Date
November 2007
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

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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