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Technology-Enabled Clinical Trials Transforming Medical Evidence Generation

机译:支持技术的临床试验转型医学证据

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The complexity and costs associated with traditional randomized, controlled trials have increased exponentially over time, and now threaten to stifle the development of new drugs and devices. Nevertheless, the growing use of electronic health records, mobile applications, and wearable devices offers significant promise for transforming clinical trials, making them more pragmatic and efficient. However, many challenges must be overcome before these innovations can be implemented routinely in randomized, controlled trial operations. In October of 2018, a diverse stakeholder group convened in Washington, DC, to examine how electronic health record, mobile, and wearable technologies could be applied to clinical trials. The group specifically examined how these technologies might streamline the execution of clinical trial components, delineated innovative trial designs facilitated by technological developments, identified barriers to implementation, and determined the optimal frameworks needed for regulatory oversight. The group concluded that the application of novel technologies to clinical trials provided enormous potential, yet these changes needed to be iterative and facilitated by continuous learning and pilot studies.
机译:与传统随机的受控试验相关的复杂性和成本随着时间的推移而增加,现在威胁要扼杀新药和设备的发展。尽管如此,越来越多地使用电子健康记录,移动应用和可穿戴设备对转化临床试验的重要承诺,使其更加务实和高效。然而,在这些创新可以在随机的,对照的试验操作中经常实施,必须克服许多挑战。 2018年10月,在华盛顿特区召开的各种利益相关方集团,以研究电子健康记录如何,移动和可穿戴技术如何应用​​于临床试验。本集团专门研究了这些技术如何简化临床试验组件的执行,划定的技术发展促进的创新试验设计,确定了实施的障碍,并确定了监管监督所需的最佳框架。本集团的结论是,将新技术应用于临床试验提供了巨大的潜力,但这些变化需要通过持续的学习和试验研究来迭代和促进。

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