Active, not recruitingNCT01800214
The Sunnybrook Dementia Study
Studying Frontotemporal dementia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Sunnybrook Health Sciences Centre
- Principal Investigator
- Sandra E Black, MD, M.DSunnybrook Health Sciences Centre
- Enrollment
- 1800 target
- Eligibility
- 40-90 years · All sexes
- Timeline
- 1995 – 2026
Study locations (1)
- Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada
Collaborators
University of Toronto · Sunnybrook Research Institute · University of Waterloo · Baycrest
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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