North American Prodromal Synucleinopathy Consortium
At a glance
Conditions
NCT03623672
Where you'd take part
This study runs at 10 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Banner Sun Health Research Institute
Sun City, Arizonano site contact published
Emory University
Atlanta, Georgiano site contact published
Massachusetts General Hospital
Boston, Massachusettsno site contact published
Mayo Clinic
Rochester, Minnesotano site contact published
McGill University
Montreal, Quebec, Canadano site contact published
Portland VA Medical Center
Portland, Oregonno site contact published
Stanford University
Redwood City, Californiano site contact published
University of California Los Angeles
Los Angeles, Californiano site contact published
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Yo-El Ju, MD · PRINCIPAL_INVESTIGATOR · Washington University School of Medicine
- Bradley Boeve, MD · PRINCIPAL_INVESTIGATOR · Mayo Clinic
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
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Inclusion
Exclusion
What this trial measures
- Prodromal Synucleinopathy Rating Scale2 years
Rating scale combining neurocognitive battery, motor, autonomic, olfaction, color vision functions. Global score range 0-3, with higher score indicating greater symptoms of synucleinopathy.