Family genetics study aims to unlock secrets of rare dementia
NCT ID NCT04639622
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 20 people from families with a genetic risk for frontotemporal dementia (FTD), including those already diagnosed and those at risk. Over five years, researchers will track changes in health and brain function to better understand how the disease develops. The goal is to gather information, not to test a treatment.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hôpital Roger Salengro, CHRU de Lille - CMRR
RECRUITINGLille, 59000, France
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