Actively Recruiting

Age: 25Years - 55Years
All Genders
Healthy Volunteers
NCT03537794

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

Age: 25Years - 55Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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.)
Not Eligible

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Unity Health Toronto

Toronto, Ontario, Canada, M5B 1M4

Actively Recruiting

Loading map...

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here