Viewing Study NCT03598868


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Study NCT ID: NCT03598868
Status: UNKNOWN
Last Update Posted: 2018-08-10
First Post: 2018-07-16
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Vortioxetine add-on Treatment Improves the Symptoms in Patients With Bipolar Depression
Sponsor: Seoul National University Hospital
Organization:

Study Overview

Official Title: Vortioxetine add-on Treatment Improves the Symptoms in Patients With Bipolar Depression
Status: UNKNOWN
Status Verified Date: 2018-08
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ViBiD
Brief Summary: The purpose of this study is to validate the efficacy of Vortioxetine augmentation in bipolar disorder patients with depressive symptoms.
Detailed 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 Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: