Nis register study comparing Seroquel and Seroquel Prolong
Study identifier:NIS-NFI-SER-2009/1
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Study Complete
Official Title
A local non interventional retrospective register study of the current clinical treatment practices and the number of hospitalization days with Seroquel or Seroquel Prolong.
Medical condition
Comparing hospitalisation time with Seroquel and Seroquel Prolong
Phase
-
Healthy volunteers
No
Study drug
-
Sex
All
Actual Enrollment
200
Study type
Observational
Age
N/A
Date
Study Start Date: 01 Aug 2009
Primary Completion Date: 01 Dec 2010
Study Completion Date: 01 Dec 2010
Study design
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verification:
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
Sponsors
AstraZeneca Pharmaceuticals
Collaborators
-
Inclusion and exclusion criteria
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No locations available
| Arms | Assigned Interventions |
|---|---|
| 1 Seroquel | - |
| 2 Seroquel Prolong | - |
Contacts
Investigators
Principal Investigator
Yrjö Ovaskainen
Medical Affairs Manager, MD, psychiatrist
