Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
2260 participants
OBSERVATIONAL
2011-11-30
2012-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RETROSPECTIVE
Study Groups
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Patients with suboptimal response
No interventions assigned to this group
Patients with symptomatic remission
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* At least 8 weeks of antidepressant treatment during the identification period of 01 January 2008 - 31 December 2009
* 18 months of enrollment with medical and pharmacy records after index episode date
18 Years
ALL
No
Sponsors
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AstraZeneca
INDUSTRY
Responsible Party
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Locations
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Research Site
Badalona, , Spain
Countries
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Other Identifiers
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NIS-NES-XXX-2011/2
Identifier Type: -
Identifier Source: org_study_id
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