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Treatment of Middle East respiratory syndrome with a combination of lopinavir/ritonavir and interferon-β1b (MIRACLE trial): statistical analysis plan for a recursive two-stage group sequential randomized controlled trial

机译:洛诺维尔/丽蒽韦和干扰素-β1B组合治疗中东呼吸综合征(奇迹试验):递归两阶段序列随机对照试验的统计分析计划

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The MIRACLE trial (MERS-CoV Infection tReated with A Combination of Lopinavir/ritonavir and intErferon-β1b) investigates the efficacy of a combination therapy of lopinavir/ritonavir and recombinant interferon-β1b provided with standard supportive care, compared to placebo provided with standard supportive care, in hospitalized patients with laboratory-confirmed MERS. The MIRACLE trial is designed as a recursive, two-stage, group sequential, multicenter, placebo-controlled, double-blind randomized controlled trial. The aim of this article is to describe the statistical analysis plan for the MIRACLE trial. The primary outcome is 90-day mortality. The primary analysis will follow the intention-to-treat principle. The MIRACLE trial is the first randomized controlled trial for MERS treatment. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02845843. Registered on 27 July 2016.
机译:奇迹试验(用Lopinavir / Ritonavir和干扰素-β1b的组合处理的MERS-COV感染)研究了与标准支持性的安慰剂相比,在标准支持性护理中提供了Lopinavir / Ritonavir和重组干扰素-β1b的组合治疗的疗效在住院治疗患者的实验室证实的MERS中。奇迹试验被设计为递归,两级,序列,多中心,安慰剂控制,双盲随机对照试验。本文的目的是描述奇迹试验的统计分析计划。主要结果是90天死亡率。主要分析将遵循意图治疗原则。奇迹试验是MERS治疗的第一个随机对照试验。试验登记:ClinicalTrials.gov,NCT02845843。 2016年7月27日注册。

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