CompletedPhase 4NCT00376051
Serotonergic Function and Behavioural and Psychological Symptoms of 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
- Sunnybrook Health Sciences Centre
- Principal Investigator
- Krista Lanctot, PhDSunnybrook Health Sciences Centre
- Intervention
- Citalopram(drug)
- Enrollment
- 22 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2006 – 2009
Study locations (2)
- Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada
- The Baycrest Centre for Geriatric Care, Toronto, Ontario, Canada
Collaborators
Alzheimer Society of Canada
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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