CompletedPhase 2NCT00200538
Efficacy and Tolerability of Memantine in Frontotemporal Dementia (FTD) Patients
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
- Nantes University Hospital
- Principal Investigator
- Martine Vercelletto, MD, M.DCentre de la Mémoire, Clinique Neurologique CHU Nord Nantes 44093 France; mvercelletto@chu-nantes.fr
- Intervention
- memantine(drug)
- Enrollment
- 52 enrolled
- Eligibility
- 45-75 years · All sexes
- Timeline
- 2005
Study locations (1)
- Martine Vercelletto, Nantes, France
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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