使用科克伦统计量的等价性研究中K 2×2表的样本量

James X Song Ph.D. , James T Wassell Ph.D.
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引用次数: 14

摘要

本文提出了一个新的Cochran测试的样本量公式,该公式使用了有关分层特定成功率的额外信息,并且需要更少的受试者进行等效研究。等效性研究在临床试验中很常见,与优势研究不同,等效性研究的目标是显示一种新药治疗是否与标准药物治疗一样有效。分层通常用于调整不同成功率的个体临床试验中心之间的差异。样本量来源于临床试验设计,其中在每个层中比较两个独立的二项比例。描述了在中心数量较大且每个中心的成功率不确切的情况下,样本量公式的实现。通过仿真显示了成功率的可变性对Cochran检验的功效的影响。成功率的可变性通过簇内相关系数来衡量,该系数可以通过Donald和Donner的ANOVA估计量来估计。模拟结果表明,与忽略分层的样本量方法相比,新样本量公式所需的对象更少。新方法提供了更大的节省,因为成功率在中心之间的可变性增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sample size for K 2×2 tables in equivalence studies using Cochran's statistic

This paper presents a new sample size formula for Cochran's test that uses additional information on stratum-specific success rates and requires fewer subjects for an equivalence study. Equivalence studies are common in clinical trials, where unlike superiority studies, the goal is to show whether a new drug therapy is as effective as a standard one. Stratification is typically used to adjust for differences among individual clinical trial centers with different success rates. The sample size is derived for a clinical trial design where two independent binomial proportions are compared within each stratum. Implementation of the sample size formula is described when the number of centers is large and the success rates of each individual center are not known exactly. The effect of variability of the success rates on the power of Cochran's test is shown through simulation. The variability of the success rates is measured by the intracluster correlation coefficient, which can be estimated by the ANOVA estimator of Donald and Donner. The simulation results show that the new sample size formula requires fewer subjects than sample size methods, which ignore stratification. The new method provides greater savings as the variability of success rates among centers increases.

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