跳至主要内容
临床试验/NCT01091038
NCT01091038已完成2 期

Improving Safety by Basic Computerizing Outpatient Prescribing

Indiana University2 个研究点 分布在 1 个国家目标入组 228 人开始时间: 2001年8月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
228
试验地点
2
主要终点
Adverse Drug Events

研究概览

简要总结

The study will measure the effect of basic clinical decision support on medical errors and adverse drug events in the ambulatory setting.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Triple (Care Provider, Investigator, Outcomes Assessor)

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •provider practicing at sites implementing order entry with basic clinical decision support using either the longitudinal medical record (LMR) or Medical Gopher

排除标准

  • •provider or practice unwilling to participate

研究组 & 干预措施

Routine Care

Placebo Comparator

Usual care of patients in the ambulatory setting

干预措施: Routine Care (Other)

Basic Clinical Decision Support

Experimental

Providers use basic clinical decision support

干预措施: Basic Clinical Decision Support (Other)

结局指标

主要结局

Adverse Drug Events

时间窗: 6 months

Adverse drug events are measured through use of a computerized surveillance system augmented by focused structured human review

Medical Errors

时间窗: 6 months

Medical Errors are identified through a computerized surveillance system with structured human review

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (2)

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