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PAT: An Intelligent Authoring Tool for Facilitating Clinical Trial Design

机译:Pat:促进临床试验设计的智能创作工具

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Great investments are made by both private and public funds and a wealth of research findings is published, the research and development pipeline phases quite low productivity and tremendous delays. In this paper, we present a novel authoring tool which has been designed and developed for facilitating study design. Its underlying models are based on a thorough analysis of existing clinical trial protocols (CTPs) and eligibility criteria (EC) published in clinicaltrials.gov by domain experts. Moreover, its integration with intelligent decision support services and mechanisms linking the study design process with healthcare patient data as well as its direct access to literature designate it as a powerful tool offering great support to researchers during clinical trial design.
机译:私人和公共资金的巨额投资以及丰富的研究结果发表,研究和开发管道阶段的生产率相当低,延迟巨大。在本文中,我们提出了一种新的创作工具,该工具已经设计和开发,以促进研究设计。其潜在的模型基于对现有的临床试验协议(CTP)和资格标准(EC)的彻底分析,在Clinicaltrials.gov通过领域专家。此外,它与智能决策支持服务和机制的集成,将研究设计过程与医疗保健患者数据相连,以及其直接访问文献指定它作为一个强大的工具,为临床试验设计中的研究人员提供了很大的支持。

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