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Clinical Trials/NCT00329810
NCT00329810
Completed
Phase 4

A Prospective, Multicenter, Open-Label Study to Evaluate the Effectiveness and the Effect on Cognitive Function of a Treatment With Aripiprazole in a Board Range of Schizophrenic Patients

ConditionsSchizophrenia
InterventionsAripiprazole

Overview

Phase
Phase 4
Intervention
Aripiprazole
Conditions
Schizophrenia
Sponsor
Otsuka Pharmaceutical Development & Commercialization, Inc.
Enrollment
500
Primary Endpoint
Clinical Global Impression scale at endpoint
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

To evaluate the effectiveness of Aripiprazole after 12 weeks of therapy for Schizophrenic patients.

Registry
clinicaltrials.gov
Start Date
March 2005
End Date
March 2006
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of Schizophrenia
  • score of 2-6 in the CGI-S scale at basline
  • ambulatory or hospitalized subjects having symptoms which requires antipsychotic treatment

Exclusion Criteria

  • women of child bearing potential
  • women pregnant or breast feeding
  • patients with a score of 0,-1 or 7
  • substance use

Arms & Interventions

Switch

Intervention: Aripiprazole

Outcomes

Primary Outcomes

Clinical Global Impression scale at endpoint

Secondary Outcomes

  • Change in Clinical Global Impression scale and cognition scales at endpoint

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