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Efficiency of study designs in diagnostic randomized clinical trials

机译:研究设计在诊断性随机临床试验中的效率

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From the patients' management perspective, a good diagnostic test should contribute to both reflecting the true disease status and improving clinical outcomes. The diagnostic randomized clinical trial is designed to combine both diagnostic tests and therapeutic interventions. Evaluation of diagnostic tests is carried out with therapeutic outcomes as the primary endpoint rather than test accuracy. We lay out the probability framework for evaluating such trials. We compare two commonly referred designs-the two-arm design and the paired design-in a formal statistical hypothesis testing setup and identify the causal connection between the two tests. The paired design is shown to be more efficient than the two-arm design. The efficiency gains vary depending on the discordant rates of test results. We derive sample size formulas for both binary and continuous endpoints. We derive estimation of important quantities under the paired design and also conduct simulation studies to verify the theoretical results. We illustrate the method with an example of designing a randomized study on preoperative staging of bladder cancer. ? 2012 John Wiley & Sons, Ltd.
机译:从患者的管理角度来看,良好的诊断测试应有助于反映真实的疾病状况和改善临床结局。诊断随机临床试验旨在将诊断测试和治疗干预措施相结合。诊断测试的评估以治疗结果为主要终点,而不是测试准确性。我们提出了评估此类试验的概率框架。我们在正式的统计假设测试设置中比较两个常用设计(双臂设计和配对设计),并确定两个测试之间的因果关系。事实证明,配对设计比两臂设计更有效。效率的提高取决于测试结果的不一致率。我们导出了二进制和连续端点的样本大小公式。我们根据配对设计得出重要数量的估计值,并进行仿真研究以验证理论结果。我们以设计一项关于膀胱癌术前分期的随机研究为例说明该方法。 ? 2012年John Wiley&Sons,Ltd.

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