CompletedPhase 2NCT02862210
Low-Dose Lithium for the Treatment of Behavioral Symptoms 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
- Columbia University
- Principal Investigator
- Edward Huey, MD, M.DBrown University
- Intervention
- Lithium Carbonate(drug)
- Enrollment
- 17 enrolled
- Eligibility
- 40-85 years · All sexes
- Timeline
- 2017 – 2022
Study locations (1)
- Columbia University Irving Medical Center, New York, New York, United States
Collaborators
Alzheimer's Drug Discovery Foundation
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.
Open NCT02862210 on ClinicalTrials.govOther trials for Frontotemporal dementia
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