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A Study Evaluating the Treatment Selection and Outcome When Changing Antipsychotic Treatment in Schizophrenic Patients (ETOS)

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Schizophrenia

Study type

Observational

Funder types

Industry

Identifiers

NCT00999895
NIS-NGR-DUM-2009/1

Details and patient eligibility

About

The purpose of the study is to evaluate the outcome of treatment switch defined as an improvement in CGI-CB scale (Clinical Global Impression - Clinical Benefit).

Enrollment

574 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of schizophrenia (as per DSM-IV), at least 6 months prior to enrolment in the study
  • Subjects who have initiated a new antipsychotic treatment within the preceding 2 weeks
  • Subjects whose prior and current antipsychotic treatment consists of any typical or atypical antipsychotic monotherapy

Exclusion criteria

  • Subjects fulfilling criteria for diagnosis of any other psychiatric condition (except from schizophrenia), as per DSM-IV Axis Ι, concomitant organic mental disorder or mental retardation
  • Substance abuse or dependence (with the exception of nicotine dependence), as defined by DSM-IV criteria and not in full remission
  • Female subjects who are pregnant or lactating

Trial design

574 participants in 1 patient group

Antipsychotic outpatients with schizophrenia
Description:
Switched treatment of antipsychotic outpatients with schizophrenia

Trial contacts and locations

43

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Data sourced from clinicaltrials.gov

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