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Trials / Completed

CompletedNCT01594996

European Drug Utilization Study

A Multinational, Multicenter, Retrospective, Observational Drug Utilisation Study of Seroquel Extended Release (XR) Prescribed by Psychiatrists as Treatment for Major Depressive Disorder (MDD) in Selected Countries in the European Union (EU)

Status
Completed
Phase
Study type
Observational
Enrollment
814 (actual)
Sponsor
AstraZeneca · Industry
Sex
All
Age
18 Years – 120 Years
Healthy volunteers
Not accepted

Summary

The purpose of this retrospective observational study is to evaluate the characteristics of patients receiving Seroquel XR as treatment for their Major Depressive Disorder. The study will also investigate how the medication is used for these patients and if there are any differences in drug utilisation between the included countries. The study is observing patients initiating Seroquel XR during a 9 month period corresponding to 3 to 12 months following the launch of the product in each country for the MDD indication. A drug utilisation questionnaire will be used to collect study data from patients' medical records.

Detailed description

A Multinational, Multicenter, Retrospective, Observational Drug Utilisation Study of Seroquel Extended Release (XR) Prescribed by Psychiatrists as Treatment for Major Depressive Disorder (MDD) in Selected Countries in the European Union (EU)

Conditions

Timeline

Start date
2012-04-24
Primary completion
2014-03-27
Completion
2014-03-27
First posted
2012-05-09
Last updated
2017-11-01

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01594996. Inclusion in this directory is not an endorsement.

European Drug Utilization Study (NCT01594996) · Clinical Trials Directory