Depression
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Subjects between the ages of 20 and 65 years at the time of consent 2) Subjects who provided informed consent by his/her free will with sufficient explanation and understanding for participation in the study 3) Subjects who meet the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) diagnostic criteria for major depressive disorder 4) Subjects who are scheduled to receive vortioxetine
Exclusion criteria
Exclusion criteria: 1) Those who have received antidepressants within the past 4 weeks 2) Patients who have or have had any of the following disorders: - Schizophrenia or other psychotic disorders - Bipolar disorder - Dementia or other neurodegenerative diseases - Substance abuse including alcohol 3) Patients with severe physical illness 4) Pregnant or lactating women or those who wish to get pregnant during the observation period of the study 5) Others who are judged to be inappropriate by the principal investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in sleep EEG during the course of treatment | — |
Countries
Japan
Contacts
Nihon University Itabashi Hospital Psychiatry