Agitation Clinical Trial
Official title:
A Double-Blind, Placebo-Controlled Evaluation of the Dexmedetomidine Transdermal Systems for Agitation Associated With Dementia of the Alzheimer's Type
The primary objective of this study is to evaluate the efficacy of DMTS on frequency and severity of agitation associated with dementia of the Alzheimer's type, compared with placebo.
This is a randomized, double-blind, placebo-controlled, two application study of DMTS or matching placebo over a 4-day treatment period, followed 7 days later with the same treatment (active or placebo) for an additional 4-day treatment period. Eligible subjects will be screened up to 7 days prior to study start. Eligible subjects will be randomized 1:1:1 to treatment with 1 DMTS, 2 DMTS, or matching placebo. ;
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