RecruitingNot ApplicableNCT02945774

Molecular Neuroimaging of Neuroinflammation in Neurodegenerative Dementias


Sponsor

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

Enrollment

40 participants

Start Date

Aug 1, 2016

Study Type

INTERVENTIONAL

Conditions

Summary

Neuroinflammation is increasingly implicated as a potential critical pathogenic mechanism in a variety of neurologic and psychiatric disorders. This study will use hybrid PET/MRI imaging to evaluate neuroinflammation and its relationship to cerebral perfusion in frontotemporal dementia (FTD). Patients with FTD will be recruited from the Cognitive Neurology and Aging Brain clinics at Parkwood Institute and will undergo neurocognitive assessment and MRI/PET using the PET ligand FEPPA which binds to activated microglia, a marker of neuroinflammation. Correlations will be conducted to determine whether abnormal neuroinflammation is present in Frontotemporal dementia and whether differential patterns of neuroinflammation are present in different FTD clinical and molecular subtypes, and to determine the relationship between neuroinflammation, cerebral perfusion using arterial spin labeling MRI imaging techniques, and indices of brain structure including volumetric and white matter analysis.


Eligibility

Min Age: 30 YearsMax Age: 95 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying (18F)-FEPPA for people with frontotemporal dementia. The study is currently recruiting participants at 1 location. People eligible for this study include aged 30 Years to 95 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

RADIATION(18F)-FEPPA

PET ligand that binds to activated microglia, a marker of neuroinflammation


Locations(1)

Parkwood Institute

London, Ontario, Canada

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NCT02945774


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