远程同意临床研究

P. Sriram
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引用次数: 2

摘要

在时间敏感和/或罕见病和重症监护试验中,临床研究试验的招募可能具有挑战性。在这些类型的临床试验中招募的障碍之一是由于同意程序,并且需要在一定时间内获得患者的同意,或者患者无法自行同意。本文将讨论在这些试验中使用远程同意选项的用法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Remote Consent Clinical Research
Recruitment in clinical research trials can be challenging in trials that are time-sensitive and/or are rare disease and critical care trials. One of the hurdles for recruitment in these types of clinical trials is due to the consent process, and the need to have consent of the patient within a certain timeframe, or the patient unable to consent for themselves. This paper will discuss the usage of the utilization of remote consent options for these trials.
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