Investigating Genetic Status in Patients Presenting to Clinic

Recruiting now

Conditions studied: Dementia, Frontotemporal, Alzheimer Dementia (AD), Lewy Body Dementia (LBD)

In brief

The causes of neurodegenerative dementias such as Frontotemporal Dementia, Lewy Body Disease and Alzheimer's disease are still largely unknown. While the contribution of some genetic mutations and polymorphisms is associated with autosomal dominant patterns of inheritance of these dementias, in many cases, the specific causative mutation in these families is not yet identified. Further, in many patients, polygenic risk is thought to give rise to pathophysiologic changes, but which specific genes affect risk are largely yet unknown. By examining genotypes in patients that present to our Cognitive Neurology and Alzheimer's Research Clinic with suspected or confirmed neurodegenerative dementia, or have a history of a familial dementia, we aim to help identify and characterize genetic mutations or polymorphisms that give rise to neurodegenerative diseases.

Key facts

Study ID
NCT05911932
Run by
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
People needed
1000
Starts
2023-10-20
Expected to finish
2043-08-01
Last updated by the study team
2025-03-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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