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Clinical Trial Summary

The purpose of this study is to validate the efficacy of Vortioxetine augmentation in bipolar disorder patients with depressive symptoms.


Clinical Trial Description

In this study, the investigators are going to examine the efficacy of vortioxetine augmentation in bipolar disorder patients with depressive symptoms.

The study design is a double-blinded 6-week prospective study. It would be useful for clinicians because it will provide new evidence for the effect of vortioxetine in bipolar disorder patients with depressive symptoms. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03598868
Study type Interventional
Source Seoul National University Hospital
Contact Sang Jin Rhee, MD
Phone 82 2 2072 2457
Email hellojr1123@hanmail.net
Status Recruiting
Phase Phase 2
Start date August 8, 2018
Completion date September 25, 2021

See also
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