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Sequential parallel comparison design with binary and time‐to‐event outcomes

机译:具有二进制和事件时间结果的顺序并行比较设计

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Sequential parallel comparison design (SPCD) has been proposed to increase the likelihood of success of clinical trials especially trials with possibly high placebo effect. Sequential parallel comparison design is conducted with 2 stages. Participants are randomized between active therapy and placebo in stage 1. Then, stage 1 placebo nonresponders are rerandomized between active therapy and placebo. Data from the 2 stages are pooled to yield a single P value. We consider SPCD with binary and with time‐to‐event outcomes. For time‐to‐event outcomes, response is defined as a favorable event prior to the end of follow‐up for a given stage of SPCD. We show that for these cases, the usual test statistics from stages 1 and 2 are asymptotically normal and uncorrelated under the null hypothesis, leading to a straightforward combined testing procedure. In addition, we show that the estimators of the treatment effects from the 2 stages are asymptotically normal and uncorrelated under the null and alternative hypothesis, yielding confidence interval procedures with correct coverage. Simulations and real data analysis demonstrate the utility of the binary and time‐to‐event SPCD.
机译:已经提出了顺序并行比较设计(SPCD)以增加临床试验成功的可能性,特别是具有高安慰剂效应的试验。顺序并行比较设计用2个阶段进行。参与者在阶段1中的活性治疗和安慰剂之间随机分配。然后,第1阶段安慰剂无反应者在活性治疗和安慰剂之间重新破坏。池中汇集来自2个阶段的数据以产生单个P值。我们考虑使用二进制和事件时间结果的SPCD。对于延时结果,响应被定义为在SPCD的给定阶段的后续行动结束之前定义为有利事件。我们表明,对于这些情况,阶段1和2的通常测试统计数据在零假设下是渐近的正常和不相关的,导致直接的组合测试程序。此外,我们表明,在2个阶段的治疗效果的估算效果在零点和替代假设下渐近正常和不相关,从而产生了正确的覆盖率的置信区间程序。模拟和实际数据分析演示了二进制和事件时间SPCD的效用。

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