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Rationale and design of a prospective substudy of clinical endpoint adjudication processes within an investigator-reported randomised controlled trial in patients with coronary artery disease: the GLOBAL LEADERS Adjudication Sub-StudY (GLASSY)

机译:研究者报告的冠心病患者随机对照试验中临床终点裁决过程的前瞻性研究的基础和设计:GLOBAL LEADERS Adjudication Sub-StudY(GLASSY)

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摘要

IntroductionThe GLOBAL LEADERS is an open-label, pragmatic and superiority randomised controlled trial designed to challenge the current treatment paradigm of dual antiplatelet therapy (DAPT) for 12 months followed by aspirin monotherapy among patients undergoing percutaneous coronary intervention. By design, all study endpoints are investigator reported (IR) and not subject to formal adjudication by an independent Clinical Event Committee (CEC), which may introduce detection, reporting or ascertainment bias.
机译:简介GLOBAL LEADERS是一项开放性,实用性和优势性随机对照试验,旨在对接受双重抗血小板治疗(DAPT)的当前治疗模式挑战12个月,然后对接受经皮冠状动脉介入治疗的患者进行阿司匹林单药治疗。通过设计,所有研究终点均由研究者报告(IR),并且不受独立临床事件委员会(CEC)的正式裁决,该委员会可能会引入检测,报告或确定性偏倚。

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