Vortioxetine 10 mg
DrugOther names: Brintellix®, Lu AA21004
NCT Number: NCT02279966
To assess the efficacy of acute treatment with 10 mg/day vortioxetine versus placebo on cognitive performance (focusing on the aspect concerning speed of processing, executive functioning, attention) in working patients with major depressive disorder (MDD).
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Notify Me18 year–65 year
All sexes
Interventional
Phase 3
EE001, Tallinn, Estonia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other protocol-defined inclusion and exclusion criteria may apply.
Other names: Brintellix®, Lu AA21004
Time frame: Baseline to Week 8
Time frame: Baseline to Week 8
Time frame: Baseline to Week 8
Time frame: Baseline to Week 8
Time frame: Baseline to Week 8
Time frame: Baseline to Week 8
Time frame: Baseline to Week 8
Time frame: Baseline to Week 8
Time frame: Baseline to Week 8
Time frame: Baseline to Week 8
Time frame: Week 8
Time frame: Baseline to Week 8
Time frame: Baseline to Week 8
H. Lundbeck A/S
Industry
An Interventional, Randomised, Double-blind, Parallel-group, Placebo-controlled, Active-referenced (Paroxetine), Fixed-dose Study on the Efficacy of Vortioxetine on Cognitive Dysfunction in Working Patients With Major Depressive Disorder
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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