drugset / Trial / NCT00200538

Efficacy and Tolerability of Memantine in Frontotemporal Dementia (FTD) Patients

NCT00200538 ↗

Phase 2 Completed 52 enrolled Nantes University Hospital
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this trial is to assess the efficacy and tolerability of memantine (anti-excitotoxic, neuroprotective treatment currently used in Alzheimer's disease \[AD\]) in frontotemporal dementia patients after a one-year treatment.

Timeline

Start
2005-09
Primary completion
—
Completion
—

Outcome

Missed primary endpoint

paper there were no significant differences between the memantine group (n = 23) and the placebo group (n = 26); p = 0.4458; PMID 21157021 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Memantine Unknown 20 mg —

Indications