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Merck

Impact of armodafinil on cognition in multiple sclerosis: a randomized, double-blind crossover pilot study.

Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology (2012-09-11)
Jared Bruce, Laura Hancock, Brandon Roberg, Amberly Brown, Erik Henkelman, Sharon Lynch
ABSTRACT

Examine the efficacy of armodafinil in improving cognition in patients with multiple sclerosis (MS). Many patients with MS experience cognitive difficulties. Armodafinil has shown promise as a cognitive enhancer in other patient populations. No studies have examined whether armodafinil improves cognition in patients with MS. We conducted a double-blind, placebo-controlled, crossover study testing the efficacy of armodafinil in reducing cognitive problems in patients with MS. We randomized 17 patients to receive a dose of lactose placebo about 2 hours before they underwent a neuropsychological testing session. After a week-long washout period, we gave them a single 250-mg dose of armodafinil about 2 hours before testing them a second time. We randomized another 16 patients to receive the active drug first, then the placebo. We excluded 3 of the participants before analyzing the data. After correcting for multiple comparisons of the 8 neuropsychological dependent measures, we found that the patients had significantly improved delayed memory on a list-learning task after they took armodafinil (P = 0.0005), but no improvement on measures of executive function, visual memory, processing speed, or self-reported fatigue. Results provide preliminary evidence that armodafinil may improve delayed verbal recall in patients with MS. A larger trial showing enhanced memory among patients taking long-term armodafinil could serve as a foundation for its possible clinical use as a memory enhancer in patients with MS.

MATERIALI
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Supelco
Modafinil solution, 1.0 mg/mL in acetonitrile, ampule of 1 mL, certified reference material, Cerilliant®
Modafinil, European Pharmacopoeia (EP) Reference Standard
Modafinil for system suitability, European Pharmacopoeia (EP) Reference Standard