Study identifier:NIS-NFR-SER-2012/1
ClinicalTrials.gov identifier:NCT01689389
EudraCT identifier:N/A
CTIS identifier:N/A
Description of the use of Quetiapine Extended Release (XR) in real-life practice in France
schizophrenia
N/A
No
-
All
2292
Observational
0 Years - 150 Years
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Dec 2015 by AstraZeneca
AstraZeneca
-
The aim of the study is to describe patient characteristics (demographic and clinical) and the patterns of use of Quetiapine XR in patients receiving the drug for the first time in real-life practice regardless the final diagnosis.
Description of the use of Quetiapine Extended Release (XR) in real-life practice in France
Location
Location
ARGENTEUIL CEDEX, France
Location
BELLEY, France
Location
CASTELMAUROU, France
Location
CAVAILLON, France
Location
LES MUREAUX, France
Location
LILLE, France
Location
MARSEILLE, France
Location
MONTPELLIER, France
Arms | Assigned Interventions |
---|---|
Main study population All eligible patients receiving Quetiapine XR for the first time in the inclusion period regardless the diagnosed disease or the patients’ age. Patients aged 18 years and over and diagnosed with bipolar disorder or schizophrenia according to DSM-IV criteria will be followed during 12 months. | - |
Schizophrenia SoC sample Patients would have to be prescribed for the first time with a new (not used during the preceding 3 months) atypical antipsychotic other than Quetiapine XR (irrespective this new atypical antipsychotic is preceded or not by another atypical antipsychotic). | - |
Bipolar SoC sample Patients would have to be prescribed a new (not used during the preceding 3 months) antidepressant [N06A], antipsychotic (other than Quetiapine XR) [N05A] or mood stabilizer (including lithium [N05AN], valproate [N03AG01], and lamotrigine [N03AX09]. | - |
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