为研究者发起的临床试验编写协议支持会议

IF 1.4 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Masaya Goto, Y. Muragaki, A. Aruga
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引用次数: 0

摘要

在研究者发起的临床试验中,采用不适当方法的方案可能会导致偏倚。然而,没有足够的数据来确定哪些项目在协议制定中是重要的或难以讨论的。我们记录了协议编写支持会议,以确定方法学家和研究者讨论了哪些项目。我们获得了所有申请人参加我们的智能临床研究与创新中心写作支持会议的批准,记录了所有的讨论,并对其进行了描述,并对项目进行了迭代整理。在一年中,我们召开了18次会议:9次早期协议会议和9次拒绝协议会议。后者被机构审查委员会拒绝,该委员会要求进行协商。讨论最多的话题是结果,占总讨论时间的20%。在三个试验中,主要问题是多重主要结局。第二个讨论最多的项目是控制。早期协议会议的非初步提案项目多于被拒绝的项目(P, 0.001)。本研究显示了研究者撰写方案的重要项目(特别是结果和控制)。早期的协议编写会议帮助研究人员发现有问题的项目。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protocol-writing support conferences for investigator-initiated clinical trials
: In investigator-initiated clinical trials, protocols with inappropriate methods might cause bias. However, insufficient data are available to determine which items are important or difficult to discuss in protocol development. We recorded protocol-writing support conferences to determine what items methodologists and investigators discussed. We obtained approval from all applicants to attend our Intelligent Clinical Research and Innovation Center writing support conferences, recorded all the discussions, characterized them, and sorted the items iteratively. In 1 year, we had 18 conferences: nine early protocol conferences and nine rejected protocol conferences. The latter were rejected by the institutional review board, which requested consultation. The most discussed item was outcomes, accounting for ∼ 20% of the total discussion time. In three trials, the main problem was multiple primary outcomes. The second most discussed item was control. Early protocol conferences had more non-preliminary proposal items than rejected ones ( P , 0.001). This study showed important items (especially outcomes and control) for investigators to write protocols. Early protocol-writing conferences helped investigators find questionable items.
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来源期刊
Open Access Journal of Clinical Trials
Open Access Journal of Clinical Trials MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.90
自引率
0.00%
发文量
2
审稿时长
16 weeks
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