Neurology & Neurosurgery Research
ALLFTD Study for Frontotemporal Lobar Degeneration (FTLD)
AGE: 18 years or older
GENDER: All
CONDITION: Frontotemporal Lobar Degeneration
GENDER: All
CONDITION: Frontotemporal Lobar Degeneration
TYPE: Observational and Biospecimen Collection Study
LOCATION: University Hospitals Cleveland Medical Center
LOCATION: University Hospitals Cleveland Medical Center
HEALTHY PARTICIPANTS: Yes, if you are a family member with a strong medical history of a FTLD syndrome you may be eligible for this study
Learn More About This Research Study
For more information, please contact study coordinator Maria Toth at 216-464-6454 option 6 or complete the online form below.
Study Purpose
The purpose of this study is to understand how Frontotemporal Lobar Degeneration (FTLD) syndromes progress over time, and to develop new tools to help with the diagnosis and eventual treatment of these syndromes.
Who Can Participate
Participants 18 years and older who are diagnosed with frontotemporal degeneration or are a family member with a strong medical history of a FTLD syndrome may be eligible for this study.
Study ID
- STUDY20200029