CompletedPhase 1NCT01386333
Safety Study of Intranasal Oxytocin 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
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
- Principal Investigator
- Elizabeth C Finger, MD, M.DUniversity of Western Ontario, Lawson Health Research Institute
- Intervention
- oxytocin(drug)
- Enrollment
- 23 enrolled
- Eligibility
- 30-80 years · All sexes
- Timeline
- 2011
Study locations (1)
- Cognitive Neurology and Alzheimer Research Centre, London, Ontario, Canada
Collaborators
Consortium of Canadian Centres for Clinical Cognitive Research
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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