Study identifier:NIS-NRU-ATC-2013/1
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Retrospective observational study to estimate the duration of initial antidepressant treatment in patients with recurrent depressive disorder who demonstrated a suboptimal response to therapy: DIANA Study
Major depressive episode
N/A
No
-
All
450
Observational
N/A
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Nov 2014 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
patients with major depression Inpatients and outpatients diagnosed with an episode of major depression relating to RDD (ICD-10, Version 2010) during the period from January 1, 2012 till September 30, 2013. Initially treated with antidepressant monotherapy, using a flexible dosage regimen if required, for at least 2 week | - |