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Nis Register Study Comparing Seroquel and Seroquel Prolong

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00965536
First Posted: August 25, 2009
Last Update Posted: February 16, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
AstraZeneca
August 24, 2009
August 25, 2009
February 16, 2011
August 2009
December 2010   (Final data collection date for primary outcome measure)
  • Hospitalisation time [ Time Frame: 2008-2010 ]
  • Treatment practice [ Time Frame: 2008-2010 ]
  • Hospitalisation time [ Time Frame: 2008-2009 ]
  • Treatment practice [ Time Frame: 2008-2009 ]
Complete list of historical versions of study NCT00965536 on ClinicalTrials.gov Archive Site
  • Primary diagnosis [ Time Frame: 2008-2010 ]
  • Medication at the end of hospitalisation [ Time Frame: 2008-2010 ]
  • GAF rating points [ Time Frame: 2008-2010 ]
  • Primary diagnosis [ Time Frame: 2008-2009 ]
  • Medication at the end of hospitalisation [ Time Frame: 2008-2009 ]
  • GAF rating points [ Time Frame: 2008-2009 ]
Not Provided
Not Provided
 
Nis Register Study Comparing Seroquel and Seroquel Prolong
A Local Non Interventional Retrospective Register Study of the Current Clinical Treatment Practices and the Number of Hospitalization Days With Seroquel or Seroquel Prolong.
The general aim of this non interventional study is to clarify what are the current clinical treatment practices of Quetiapine Immediate Release and Quetiapine Extended Release. The primary objectives of the study are:1.To collect information on the used Quetiapine Immediate Release or Quetiapine Extended Release medication 2.To collect information on duration and number of hospitalisation days 3.Change of GAF points
Not Provided
Observational
Observational Model: Case Control
Time Perspective: Retrospective
Not Provided
Not Provided
Probability Sample
South Karelia Central Hospital in-patients
Comparing Hospitalisation Time With Seroquel and Seroquel Prolong
Not Provided
  • 1
    Seroquel
  • 2
    Seroquel Prolong
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
200
December 2010
December 2010   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Medication: Seroquel or Seroquel Prolong
  • Diagnosis: F20-F29 or F30-F31 (ICD-10)
  • In-patient

Exclusion Criteria:

Sexes Eligible for Study: All
Child, Adult, Senior
No
Contact information is only displayed when the study is recruiting subjects
Finland
 
 
NCT00965536
NIS-NFI-SER-2009/1
No
Not Provided
Not Provided
MC MD, AstraZeneca
AstraZeneca
Not Provided
Study Director: Yrjö Ovaskainen Medical Affairs Manager, MD, psychiatrist
Principal Investigator: Kari Hänninen MD, psychiatrist
AstraZeneca
February 2011
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