A Double-Blind, Placebo-Controlled Study of Memantine in the Treatment of Major Depression
Memantine
Depression
Placebo-controlled study
DOI:
10.1176/appi.ajp.163.1.153
Publication Date:
2006-01-03T17:03:00Z
AUTHORS (8)
ABSTRACT
OBJECTIVE: This study was designed to assess possible antidepressant effects of memantine, a selective N-methyl-D-aspartate (NMDA) receptor antagonist in humans. METHOD: In double-blind, placebo-controlled study, 32 subjects with major depression were randomly assigned receive memantine (5–20 mg/day) (N=16) or placebo for 8 weeks. Primary efficacy assessed by performance on the Montgomery-Åsberg Depression Rating Scale (MADRS). RESULTS: The linear mixed models total MADRS scores showed no treatment effect. CONCLUSIONS: an 8-week trial, low-to-moderate-affinity NMDA doses 5–20 mg/day not effective depressive disorder.
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