Actively Recruiting
Characterizing Dopamine Receptor Binding in Treatment Resistant Depression
Led by Unity Health Toronto · Updated on 2026-03-16
45
Participants Needed
1
Research Sites
171 weeks
Total Duration
On this page
Sponsors
U
Unity Health Toronto
Lead Sponsor
C
Centre for Addiction and Mental Health
Collaborating Sponsor
AI-Summary
What this Trial Is About
It is estimated that 30% of individuals with Major Depressive Disorder (MDD) fail to respond to conventional antidepressant medication which accounts for over 1 million Canadians in their lifetime. Treatment resistant depression (TRD) patients also have greater psychiatric and medical comorbidity, poorer quality of life and increased suicidal ideation. Yet, there are few treatment strategies available to target TRD and there is a significant lack of evidence about how TRD differs from treatment-responsive depression. This proposal represents the first study to elucidate the neurobiology of TRD with a focus on dopamine receptor function throughout the brain, in order to inform treatment development and clinical characterization of TRD.The ultimate goal of this unique study is to characterize striatal and extrastriatal dopamine D2 and D3 receptor binding potential in patients with TRD, non-resistant MDD and healthy controls. The primary hypothesis is that TRD patients will exhibit greater D2/D3 receptor binding potential compared to non-TRD patients in the following regions of interest: dorsolateral prefrontal cortex, orbitofrontal cortex, and ventral striatum. Secondarily, non-TRD patients will also demonstrate increased binding potential compared to healthy controls in the same brain regions. Whole brain analyses will allow us to take an exploratory approach to other brain regions that may differentiate TRD from non-TRD patients. Participants will be assessed at St. Michael's Hospital (SMH) and the Centre for Addiction and Mental Health (CAMH), which are within a 10 minute driving distance of each other. There will be 3 study visits following written informed consent. Eligibility will be confirmed at a screening visit at SMH where demographic information, including age, sex, education, and medication history will be obtained, as well as the administration of a structured Mini-International Neuropsychiatric Interview (MINI) for Diagnostic and Statistical Manual of Mental Disorders (DSM-5) Axis I diagnoses (Sheehan et al, 2015), and an HRSD-17. Within two weeks of the screening visit, participants will undergo a structural magnetic resonance imaging (MRI) scan at SMH prior to the positron-emission tomography (PET) scan at CAMH. The order of the PHNO scans will be counterbalanced.
CONDITIONS
Official Title
Characterizing Dopamine Receptor Binding in Treatment Resistant Depression
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of Major Depressive Episode within Major Depressive Disorder confirmed by MINI
- Age between 25 and 55 years
- Hamilton Depression Rating Scale (17 item) score greater than 14
- Free of psychotropic medications for at least 5 half-lives before PET scanning
- Ability to safely undergo MRI scanning (no metal, pacemakers, etc.)
- For non-resistant patients: history of positive response to antidepressants
- For healthy controls: age between 25 and 55 years
- For healthy controls: ability to safely undergo MRI scanning (no metal, pacemakers, etc.)
You will not qualify if you...
- Pregnancy or lactation
- Medical condition needing immediate treatment
- Recent (less than 6 months) or current drug abuse or dependence
- Lifetime history of psychosis (for MDD patients)
- Use of any psychotropic medication within 5 half-lives before PET scanning
- For non-resistant patients: failure of more than 2 adequate antidepressant treatments for current episode
- For healthy controls: any lifetime psychiatric disorder
- For healthy controls: any lifetime use of antidepressants
AI-Screening
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Trial Site Locations
Total: 1 location
1
Unity Health Toronto
Toronto, Ontario, Canada, M5B 1M4
Actively Recruiting
Research Team
S
Sakina J Rizvi, PhD
CONTACT
A
Ariel Graff-Guerrero, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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