Last updated on October 2020

Real-life Effectiveness of Vortioxetine in Depression

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Major depression | Endogenous depression
  • Age: Between 18 - 100 Years
  • Gender: Male or Female

Inclusion Criteria:

  • The patient is 18 years
  • The patient is an outpatient, treated in a GP or psychiatric outpatient practice
  • The patient has a diagnosis of major depressive episode according to local diagnostic criteria
  • The patient has been prescribed vortioxetine according to the local Summary of Product Characteristics (SmPC)

Exclusion Criteria:

  • The patient is unable to read and understand the information sheet and informed consent form or the Patient Reported Outcomes (PRO)
  • The patient is concurrently participating in a clinical trial
  • The patient has a diagnosis of schizophrenia or other psychotic disorder according to local diagnostic criteria
  • The patient has a diagnosis of bipolar disorder according to local diagnostic criteria
  • The patient has a substance use disorders other than tobacco use disorder
  • The patient has dementia or other neurodegenerative disease significantly impacting cognitive functioning
  • The patient has a mood disorder due to a general medical condition or substances
  • The patient is pregnant, 6 months post-partum or breastfeeding
  • The patient is at significant risk of suicide in the investigator's opinion or the patient has attempted suicide within the last six months
  • The patient is a member of the study personnel or of their immediate families, or is a subordinate (or immediate family member of a subordinate) to any of the study personnel

Recruitment Status: Closed

Brief Description Eligibility Contact Research Team

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