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ABSTRACT: Objective
To evaluate the efficacy and safety of bupropion in the treatment of apathy in Huntington's disease (HD).Methods
In this phase 2b multicentre, double-blind, placebo-controlled crossover trial, individuals with HD and clinical signs of apathy according to the Structured Clinical Interview for Apathy-Dementia (SCIA-D), but not depression (n = 40) were randomized to receive either bupropion 150/300mg or placebo daily for 10 weeks. The primary outcome parameter was a significant change of the Apathy Evaluation Scale (AES) score after ten weeks of treatment as judged by an informant (AES-I) living in close proximity with the study participant. The secondary outcome parameters included changes of 1. AES scores determined by the patient (AES-S) or the clinical investigat
SUBMITTER: Gelderblom H
PROVIDER: S-EPMC5360242 | biostudies-literature | 2017
REPOSITORIES: biostudies-literature