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CompletedNCT01342120

PHARMO Institute Seroquel Safety Study

Seroquel Safety Study

Status
Completed
Phase
Study type
Observational
Enrollment
18,325 (actual)
Sponsor
AstraZeneca · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this observational study is to study specific outcomes of interest in users of quetiapine compared with all other atypical antipsychotics and specifically olanzapine and risperidone. The outcomes of interest are all-cause mortality, failed suicide attempts, extrapyramidal symptoms, diabetes mellitus, hypothyroidism, acute myocardial infarction and stroke. This retrospective cohort study is based on population-based record linkage system (PHARMO RLS) capturing about 2.5 millions residents in the Netherlands.

Conditions

Timeline

Start date
2010-09-01
Primary completion
2010-11-01
Completion
2010-11-01
First posted
2011-04-27
Last updated
2011-09-02

Source: ClinicalTrials.gov record NCT01342120. Inclusion in this directory is not an endorsement.

PHARMO Institute Seroquel Safety Study (NCT01342120) · Clinical Trials Directory