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临床试验/NCT00393562
NCT00393562撤回不适用

Comparison of Modafinil and Methylphenidate in Treatment of Excessive Daytime Sleepiness in Patients With Parkinson's Disease

US Department of Veterans Affairs2 个研究点 分布在 1 个国家开始时间: 2006年3月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
撤回
试验地点
2
主要终点
Compare efficacy of the two agents in treating excessive daytime sleepiness at 4 and 8 weeks

研究概览

简要总结

This is an open-label cross-over randomized control study comparing the effect of modafinil and methylphenidate in patients with Parkinson's disease with excessive daytime sleepiness.

详细描述

Sleep disorders are common in Parkinson's disease (PD) and a significant cause of impairment of function in already disabled individuals. Almost all patients with PD report disturbed sleep, including excessive daytime sleepiness (EDS), disorders of initiating and maintaining sleep (DIMS) or parasomnias.1 The underlying pathology associated with PD and medication effects have both been implicated in the sleep disorders affecting these patients. EDS has become the focus of attention because of its effect on quality of life and impairment in driving and predisposition to traffic accidents. Its prevalence has been estimated between 15-50%. Treatment of EDS has become an important factor in the management of the PD patient, and the recent introduction of modafinil, a wakefulness promoting agent approved for narcolepsy, has led to increasing off-label use of this agent. Prior to modafinil, amphetamine and methylphenidate, two classical psychostimulants, were the agents of choice in treating EDS. However, these agents also have a direct effect on the dopaminergic system. They increase both sleep and REM latency, while reducing total sleep time and REM sleep. By comparison, the mechanism of action of modafinil is unknown, yet distinct from that of the psychostimulants. A direct comparison of the effect on EDS of modafinil with classical psychostimulants is lacking. The overall goals of this research proposal are to determine which agent is most effective in treating EDS in PD patients by using an open-label randomized control study comparing efficacy, onset of action and tolerability.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
50 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Veteran at study site

排除标准

  • Patients unable to give consent
  • Diagnosis of EDS prior to diagnosis of PD
  • Brain injury due to trauma, CVA, tumor or anoxia

结局指标

主要结局

Compare efficacy of the two agents in treating excessive daytime sleepiness at 4 and 8 weeks

次要结局

  • Compare the safety profile of modafinil and methylphenidate

研究者

申办方类型
Fed

研究点 (2)

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