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Clinical trials in ALS: A review of the role of clinical and neurophysiological measurements

机译:ALS中的临床试验:临床和神经生理学测量作用的综述

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We have reviewed all the published clinical trials of ALS and, from those considered sufficiently large, and containing a control group, we have evaluated their methodology with regard to statistical power. This implies a critical analysis of the endpoint measurements. We have concluded that clinical endpoints used in clinical trials of ALS have frequently been insufficiently sensitive, non-linear, or even not intuitively highly relevant to the disease. We suggest that the ALS-FRS, perhaps also MUNE and the Neurophysiological Index, may be the best measures currently available. These techniques have complementary characteristics that allow them to be used to address different aspects of the disease and its treatment in various trials designs. In the past some trials may have failed to demonstrate a treatment effect because the chosen endpoint measures and the trial design were inappropriate.
机译:我们已经审查了所有已发表的ALS临床试验,并且从那些被认为足够大并包含对照组的试验中,我们评估了其统计功效的方法。这意味着对端点测量进行了严格的分析。我们已经得出结论,用于ALS的临床试验中的临床终点常常与该疾病的敏感性,非线性或什至不是直观上高度相关。我们建议ALS-FRS,也许还有MUNE和神经生理学指数,可能是目前可用的最佳方法。这些技术具有互补的特性,使它们可以用于各种试验设计中疾病的不同方面及其治疗。在过去,某些试验可能未能证明治疗效果,因为选择的终点指标和试验设计不合适。

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