全面的网上收集系统。

L Kowitt, R L Marlin
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引用次数: 1

摘要

在临床药物试验的正常进行中,从药物反应数据的收集点(通常是通过在每位患者就诊时填写的标准书面病例报告表格)到将其输入申办者机构的计算机系统(随后可用于评估)之间存在相当长的时间滞后。这种滞后期可能从几天到一个月或几个月不等。以前通过在临床研究者办公室提供电子数据输入能力来减少这一时间跨度的努力,由于复杂性和相对不准确的原因,通常被证明是不令人满意的。本文将描述最近开发的一种可能解决这整个问题的方法。它涉及提供一台装有精密的定制数据输入软件的微型计算机,以提供一种手段,大大减少这一长期拖延完成临床药物试验的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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A comprehensive on-line collection system.

In the normal conduct of a clinical drug trial, a considerable time lag exists between the point when drug response data are collected, usually by means of a standard written case report form completed at the time of an individual patient visit, and the time when it is entered into the computer system (and thereafter available for assessment) in the sponsor 's facility. This lag period may range from a matter of days to one or several months. Previous efforts to reduce this time span by providing electronic data entry capability within the clinical investigator's office have generally proven unsatisfactory for reasons of complexity and relative inaccuracy. A recently-developed potential solution to this entire problem will be described. It involves the provision of a microcomputer equipped with sophisticated customized data entry software that offers a means to substantially reduce this long-standing source of delays in the completion of clinical drug trials.

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来源期刊
Drug Information Journal
Drug Information Journal 医学-卫生保健
自引率
0.00%
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审稿时长
6-12 weeks
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