Evaluation of the Fill-it-up-design to use historical control data in randomized clinical trials with two arm parallel group design

IF 3.9 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Stephanie Wied, Martin Posch, Ralf-Dieter Hilgers
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Abstract

In the context of clinical research, there is an increasing need for new study designs that help to incorporate already available data. With the help of historical controls, the existing information can be utilized to support the new study design, but of course, inclusion also carries the risk of bias in the study results. To combine historical and randomized controls we investigate the Fill-it-up-design, which in the first step checks the comparability of the historical and randomized controls performing an equivalence pre-test. If equivalence is confirmed, the historical control data will be included in the new RCT. If equivalence cannot be confirmed, the historical controls will not be considered at all and the randomization of the original study will be extended. We are investigating the performance of this study design in terms of type I error rate and power. We demonstrate how many patients need to be recruited in each of the two steps in the Fill-it-up-design and show that the family wise error rate of the design is kept at 5 $$\%$$ . The maximum sample size of the Fill-it-up-design is larger than that of the single-stage design without historical controls and increases as the heterogeneity between the historical controls and the concurrent controls increases. The two-stage Fill-it-up-design represents a frequentist method for including historical control data for various study designs. As the maximum sample size of the design is larger, a robust prior belief is essential for its use. The design should therefore be seen as a way out in exceptional situations where a hybrid design is considered necessary.
评估在双臂平行组设计的随机临床试验中使用历史对照数据的 "填表--补题--设计 "方法
在临床研究中,越来越需要有助于纳入现有数据的新研究设计。在历史对照的帮助下,现有信息可以用来支持新的研究设计,当然,纳入历史对照也会带来研究结果偏差的风险。为了将历史对照和随机对照结合起来,我们研究了 "填充式设计"(Fill-it-up-design),该设计的第一步是检查历史对照和随机对照的可比性,并进行等效性预测试。如果等效性得到确认,历史对照数据将被纳入新的 RCT。如果无法确认等效性,则完全不考虑历史对照,并延长原始研究的随机化时间。我们正在研究这种研究设计在 I 型错误率和功率方面的表现。我们演示了在 "填-补 "设计的两个步骤中,每个步骤需要招募多少病人,并表明该设计的家系误差率保持在 5 $$\%$$。填充-向上-设计的最大样本量大于无历史对照的单阶段设计,并且随着历史对照和同期对照之间异质性的增加而增加。两阶段 "填平补齐 "设计是将历史对照数据纳入各种研究设计的一种频繁主义方法。由于该设计的最大样本量较大,因此使用该设计必须要有可靠的先验信念。因此,在需要采用混合设计的特殊情况下,应将该设计视为一种出路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Medical Research Methodology
BMC Medical Research Methodology 医学-卫生保健
CiteScore
6.50
自引率
2.50%
发文量
298
审稿时长
3-8 weeks
期刊介绍: BMC Medical Research Methodology is an open access journal publishing original peer-reviewed research articles in methodological approaches to healthcare research. Articles on the methodology of epidemiological research, clinical trials and meta-analysis/systematic review are particularly encouraged, as are empirical studies of the associations between choice of methodology and study outcomes. BMC Medical Research Methodology does not aim to publish articles describing scientific methods or techniques: these should be directed to the BMC journal covering the relevant biomedical subject area.
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