首页> 外文期刊>Contemporary Clinical Trials Communications >Determining a Bayesian predictive power stopping rule for futility in a non-inferiority trial with binary outcomes
【24h】

Determining a Bayesian predictive power stopping rule for futility in a non-inferiority trial with binary outcomes

机译:用二元成果确定徒劳无功的无劣次审判中徒劳无功的预测力

获取原文
           

摘要

Background/AimsNon-inferiority trials investigate whether a novel intervention, which typically has other benefits (i.e., cheaper or safer), has similar clinical effectiveness to currently available treatments. In situations where interim evidence in a non-inferiority trial suggests that the novel treatment is truly inferior, ethical concerns with continuing randomisation to the “inferior” intervention are raised. Thus, if interim data indicate that concluding non-inferiority at the end of the trial is unlikely, stopping for futility should be considered. To date, limited examples are available to guide the development of stopping rules for non-inferiority trials.MethodsWe used a Bayesian predictive power approach to develop a stopping rule for futility for a trial collecting binary outcomes. We evaluated the frequentist operating characteristics of the stopping rule to ensure control of the Type I and Type II error. Our case study is the Intranasal Ketamine for Procedural Sedation trial (INK trial), a non-inferiority trial designed to assess the sedative properties of ketamine administered using two alternative routes.ResultsWe considered implementing our stopping rule after the INK trial enrols 140 patients out of 560. The trial would be stopped if 12 more patients experience a failure on the novel treatment compared to standard care. This trial has a type I error rate of 2.2% and a power of 80%.ConclusionsStopping for futility in non-inferiority trials reduces exposure to ineffective treatments and preserves resources for alternative research questions. Futility stopping rules based on Bayesian predictive power are easy to implement and align with trial aims.Trial registrationClinicalTrials.gov NCT02828566 July 11, 2016.
机译:背景/ Aimsnon-Deveriosity试验研究了是否具有其他益处(即便宜或更安全)的新型干预,对目前可用治疗具有类似的临床效果。在非劣级审判中的临时证据表明新的治疗真正劣等的情况下,提出了持续随机化对“劣质”干预的伦理问题。因此,如果临时数据表明在试验结束时结束非较低的情况不太可能,则应考虑停止徒劳无功。迄今为止,有限的例子可用于指导非卑鄙试验停止规则的制定。近奇地区使用了贝叶斯预测电力方法来制定停止规则,以便进行收集二元成果的审判。我们评估了停止规则的频繁操作特性,以确保控制I型和II型错误。我们的案例研究是用于程序镇静试验(墨水试验)的鼻内氯胺酮,旨在评估使用两种替代路线管理的氯胺酮的镇静性质。墨水审判患者在墨水审判中的140名患者之后考虑实施我们的停止规则的镇静性试验。 560.如果12名患者与标准护理相比,12名患者在新型治疗中经历失败,则会停止审判。该试验的I型错误率为2.2%,功率为80%。合适的非劣效性试验中的无用率可减少导致无效的处理,并为替代研究问题提供资源。基于贝叶斯预测电力的无人机停止规则很容易实现并与试用瞄准符合对齐.TRIAL NCTERINGCLINICTRIALS.GOV NCT02828566 2016年7月11日。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号