NCT02790970
Who may be able to join
Who might be able to join this trial:
- You are a male or female aged between 18 and 70 years old (inclusive).
- You have been diagnosed by a doctor with a depressive episode (either your first episode or a returning one) that needs to be treated with a type of antidepressant called an SSRI (but not the specific SSRI called fluoxetine).
- A doctor has prescribed you an SSRI for depression within the last 7 days before your first visit to the trial site, but you have not yet started taking it.
- You are planning to start taking your SSRI within 7 days of your first visit to the trial site.
Who may not be able to join:
- You have a history of mania (a period of abnormally high mood or energy) at any point in the past.
- You are currently taking any antidepressant medication, or you stopped taking an antidepressant less than 2 weeks before your first visit to the trial site.
- Your doctor feels you need to be referred to specialist or higher-level mental health services rather than being treated in a standard setting (confirm with trial site).
- You are currently experiencing significant thoughts of suicide that require extra care and monitoring from your doctor.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Trial details
Where this trial is recruiting
Primary endpoints
Increase in proportion of depressed patients showing a response to treatment at week 8 when using the PReDicT Test to direct antidepressant treatment compared to treatment as usual as measured by the QIDS-SR-16
Can't join this trial?
Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.