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Molecular Imaging of Brain Inflammation in Depressive Disorders

Molecular Imaging of Brain Inflammation in Depressive Disorders

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02983318
Acronym
DiME
Enrollment
20
Registered
2016-12-06
Start date
2017-08-28
Completion date
2019-12-31
Last updated
2020-04-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depressive Disorder, Major, Positron-Emission Tomography

Brief summary

In a number of neuropsychiatric disorders such as depression, both brain inflammation and glutamate mediated excitotoxicity (cell death through over-activated stimulation) are suspected to play a key role. It is difficult, if not impossible, to determine the potential destructiveness of the inflammatory response seen in disease states by studying the brain's inflammatory cells (microglia) activity in isolation. The investigators are proposing to develop the means to concurrently study inflammatory response (i.e., microglial activity) and its potentially devastating consequence (i.e., glutamate excitotoxicity) across the entire brain in order to establish the importance of inflammation. In this study the investigators propose a phased clinical study whereby the early-phase involves the development of our capacity to study inflammation-mediated damage to brain cells, followed by a feasibility study in patients with clinical depression that tests whether concurrent inflammation and glutamate excess could be measured in key brain regions associated with a depressed mood state.

Interventions

None listed

Sponsors

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
19 Years to 105 Years
Healthy volunteers
Yes

Inclusion criteria

* screening form for MRI/PET is satisfactory after being reviewed by a radiologist * diagnosed with depression or healthy control participants with no present mental health disorder * Good general health with no diseases expected to interfere with the study * Subject is not pregnant, lactating, or of childbearing potential (must be practicing effective form of birth control) * Patient and healthy controls must not have an infection or an autoimmune disorder or persistent inflammation.

Exclusion criteria

* Any significant systemic illness or unstable medical condition which could lead to difficulty complying with the protocol * use of Investigational agents within last month

Design outcomes

Primary

MeasureTime frameDescription
inflammation-related excitotoxicity in the brainsingle time. Data collected at baseline with no follow up.Cross sectional MRI/PET scan will be used to identify inflammation related excitotoxicity in the brain in healthy individuals and those diagnosed with major depression.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026