Status:

COMPLETED

Efficacy and Safety of SEROQUEL Extended Release (XR) in Acute Schizophrenia

Lead Sponsor:

AstraZeneca

Conditions:

Schizophrenia

Eligibility:

All Genders

18-65 years

Phase:

PHASE4

Brief Summary

The purpose of the study is to determine whether treatment with quetiapine XR (Seroquel XR) tablets for 3 weeks will improve their agitation when they have acute psychosis.

Eligibility Criteria

Inclusion

  • Requirement for treatment of acute episode of schizophrenia (according to DSM-IV diagnostic criteria)
  • PANSS total score of ³ 75
  • CGI \> 4

Exclusion

  • Any DSM-IV (Diagnostic and Statistical Manual of Mental Disorders 4th Edition) Axis I disorder not defined in the inclusion criteria
  • Patients who, in the opinion of the investigator, pose an imminent risk of suicide or a danger to self or others
  • Substance or alcohol dependence at enrollment

Key Trial Info

Start Date :

September 1 2009

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

April 1 2010

Estimated Enrollment :

35 Patients enrolled

Trial Details

Trial ID

NCT00954122

Start Date

September 1 2009

End Date

April 1 2010

Last Update

January 8 2013

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Research Site

Johor Bahru, Johor Bahru, Malaysia

2

Research Site

Kuala Lumpur, Malaysia

Efficacy and Safety of SEROQUEL Extended Release (XR) in Acute Schizophrenia | DecenTrialz