CompletedPhase 3NCT00594737
Open Label Pilot Study of the Effects of Memantine on FDG-PET in Frontotemporal Dementia
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
- Tiffany Chow, MD
- Principal Investigator
- Tiffany W Chow, MD, M.DRotman Research Institute at Baycrest, University of Toronto
- Intervention
- memantine hydrochloride(drug)
- Enrollment
- 17 enrolled
- Eligibility
- 40-80 years · All sexes
- Timeline
- 2007 – 2012
Study locations (1)
- Baycrest, Toronto, Ontario, Canada
Collaborators
H. Lundbeck A/S
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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