Study identifier:NIS-NDK-SER-2010/2
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A retrospective, non-interventional study to evaluate the use of Seroquel XR and Seroquel IR in the clinical practice of outpatients with schizophrenia
schizophrenia
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No
-
All
186
Observational
18 Years - 65 Years
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Mar 2011 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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The primary objective of this non-interventional study is to investigate how Seroquel XR and Seroquel IR are used in the clinical practice of outpatients with schizophrenia. This will be done by a retrospective review of medical records to evaluate patients treated with Seroquel XR or Seroquel IR as primary antipsychotic treatment.
Location
Location
Aabenraa, Aabenraa, Denmark
Location
Arhus, Arhus, Denmark
Location
Cph N, Cph, Denmark
Location
Cph NV, Cph, Denmark
Location
Arhus N, Arhus, Denmark
Location
Arhus S, Arhus, Denmark
Location
Hillerod, Hillerod, Denmark
Location
Ballerup, Ballerup, Denmark
Arms | Assigned Interventions |
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300 patients Female or male aged 18-65 years with a diagnosis of schizophrenia having received at least one dose of Seroquel XR or Seroquel IR during January – March 2010 | - |
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