超越安慰剂:罕见疾病研究中随机对照试验设计的替代方案

P. Sriram
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引用次数: 2

摘要

罕见病和孤儿病指征在临床试验中可能出现独特的困难和挑战。针对罕见病的试验遇到的一些挑战可能包括招募和登记。对于罕见病试验中遇到的挑战,其中一个解释是由于研究的试验设计,将研究产品与安慰剂进行比较。这篇综述文章讨论了安慰剂的使用,以及在制定方案时何时可以考虑其他选择,特别是考虑到罕见疾病的研究。对于研究者和那些设计方案的人来说,考虑标准随机对照试验的替代方案是至关重要的。本文的目的是回顾可选的试验设计方案。本综述中讨论的试验设计包括交叉试验、单臂研究和历史数据以及n-of-1试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Beyond Placebo: Alternative Options to the Randomized Control Trial Design in Rare Disease Studies
Unique difficulties and challenges can arise for rare diseases and orphan disease indications within a clinical trial. Some of the challenges encountered by trials that are working on rare diseases can include recruitment and enrollment. One of the explanations for the challenges that are encountered in rare disease trials is because of the trial design of study, where the investigational product is being compared to the placebo. This review paper discusses the usage of placebo and when other options could be taken into consideration while creating the protocol, specifically with consideration to rare disease studies. It is essential for the investigators and those designing the protocol to consider alternative options from the standard randomized controlled trial. The aim of this paper is to review alternative trial design options. The trial designs discussed in this review paper include crossover trials, single arm studies and historical data, and n-of-1 trials.
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