生物等效性研究的样本量建议

IF 1.6 Q1 STATISTICS & PROBABILITY Statistica Pub Date : 2017-04-07 DOI:10.6092/ISSN.1973-2201/6699
C. Bhupathi, Venakata HaraGopal Vajjha
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引用次数: 6

摘要

卫生当局(HA)对健康志愿者(HV)的生物等效性(BE)研究的样本量和功率计算有明确的指导和建议。建议功率至少为80%,类型1误差为5%。在现实生活情况下,临床试验计划率超过80%,样本量更大。权力的增加意味着更多的受试者,更多的时间浪费和更多的资源来完成研究,从而导致更多的资金花费。本文试图展示在不影响研究的科学有效性的情况下可以实现多少样本量的减少,以及对减少样本量对资源(受试者,时间,血液和成本)的总体影响的简要总结。我们进行了模拟,以显示对功率的影响,并使用双侧置信区间方法来显示研究的等效性或其他。为了说明目的,考虑了两个时期的交叉研究。采用不同样本量进行了100次模拟,与原始结果进行比较。
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Sample size recommendation for a bioequivalent study
There are clear guidelines and suggestions on the sample size and power calculation from health authorities (HA) for Bio equivalence (BE) studies in Healthy volunteers (HV). The suggested power is at least 80\% and type 1 error is 5\%. In real life situations, the clinical trials plan with more than 80\%, giving rise to larger sample size. The increased power means more subjects, more wastage of time and more resources to complete the study, resulting in more money spent. This paper attempts to show how much reduction in the sample size can be achieved without affecting the scientific validity of the study and also the brief summary on the overall effect of reduced sample size on resources (subjects, time, blood and cost). We executed simulations in order to show the impact on the power and the 2 one sided confidence interval approach to show the study equivalence or otherwise. For illustration purpose, a couple of 2 period cross over studies were considered. 100 simulations were executed with different sample sizes to compare with the original results.
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来源期刊
Statistica
Statistica STATISTICS & PROBABILITY-
CiteScore
1.70
自引率
0.00%
发文量
0
审稿时长
10 weeks
期刊最新文献
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