A Phase 2 Clinical Trial of Intranasal Oxytocin for Frontotemporal Dementia
Principal Investigator
Ging-Yuek Robin HsiungOverview
Study Start/End
May 11, 2018 to Dec 31, 2020Locations
UBC HospitalName/Title
Tahlee Marian, Study CoordinatorPhone
604-822-0324Email Address
tahlee.marian@vch.caPurpose of Study
The purpose of this study is to assess the safety, tolerability and effects on behaviour of Syntocinon given intranasally (by a spray into the nostrils) compared to placebo (an inactive saline substance that contains no medication) in participants with frontotemporal dementia/Pick's disease.
Eligibility
Visit ClinicalTrials.gov for more information.
Disclaimer
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