Presynaptic Imaging in Major Depressive Episodes After COVID-19
Recruiting now NCT06086366
Run by Centre for Addiction and Mental Health · for 18 to 75 · All sexes · accepts healthy volunteers
What this study is about
The goal of this observational study focuses on understanding and addressing a subset of persistent neuropsychiatric symptoms occurring within 3 months after mild to moderate COVID-19 infection (COVID-DNP). COVID-DNP encompasses major depressive episodes (MDE) with or without additional neuropsychiatric symptoms.
Who can join (things the study team will check)
✅ You may be able to join if…
- New onset MDE within 3 months after mild or moderate COVID-19, with MDE verified by the research version SCID for DSM 5. See "Positive COVID-19 diagnosis" listed after inclusion/exclusion criteria for a description of how this is determined.
- Age 18 to 75.
- Good general physical health with no active medical conditions based on self-report (except migraine or PASC).
🚫 You may not be able to join if…
- Use of antidepressants in the previous month (6 weeks for fluoxetine).
- Use of stimulant medication affecting dopamine release in the previous month
- Use of antipsychotics in the previous month
- History of neurological disease (except migraine, and PASC) based on self-report
- Use of medications or herbal products or natural health products with central nervous system effects in past 2 weeks based on self-report
- Presence of cigarette smoking in the past two months, based on self-report
- Lifetime diagnosis of severe Substance or Alcohol Use Disorder, or diagnosis of mild to moderate Substance or Alcohol Use Disorder in the past two years, based on self-report and verified by the Research Version of Structured Clinical Interview for Diagnostic and Statistical Manual-5 (SCID-5-RV)
- Use of recreational drugs, including marijuana, in the past two months, based on self-report and verified by the Research Version of Structured Clinical Interview for Diagnostic and Statistical Manual-5 (SCID-5-RV)
- Positive urine drug or cotinine screen at any timepoint during the study
- History of psychotic symptoms secondary to schizophrenia, schizophreniform, bipolar disorder, or brief psychotic disorder prior to COVID-19, based on self-report and verified by the Research Version of Structured Clinical Interview for Diagnostic and Statistical Manual-5 (SCID-5-RV)
- Currently pregnant, based on self-report or positive pregnancy test at any timepoint during the study, in females (in our PET Centre females up to 65 years of age are given a urine pregnancy test prior to every PET scan)
- Breastfeeding (for females)
- Current disorders of coagulation, blood or ongoing use of anticoagulant medication, based on self-report
- Claustrophobia, based on self-report
- Weight over 400lbs and height over 7ft (requirements for fitting in the scanners and hospital gowns)
- Presence of metal implant, object or electrical devices that are contraindicated for MRI, based on self-report
- Severe allergic reaction to alcohol
Where this trial is running
- Centre for Addiction and Mental Health, Toronto, Ontario, Canada
Who to contact
Karida Liu · 416-535-8501 · liuyuhan0830@gmail.com
It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT06086366.
Verify everything on the official ClinicalTrials.gov record. Page updated July 2026.
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