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临床试验/NCT00013143
NCT00013143已完成不适用

Patient Profiling and Provider Feedback to Reduce Adverse Drug Events

US Department of Veterans Affairs2 个研究点 分布在 1 个国家目标入组 1,200 人开始时间: 2001年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
1,200
试验地点
2

研究概览

简要总结

Adverse drug events (ADE) present a unique focus for error reduction. Computerized provider order entry, with embedded clinical decision support, has great promise in reducing medication errors but preventable adverse drug events may still occur despite such systems.

详细描述

Background:

Adverse drug events (ADE) present a unique focus for error reduction. Computerized provider order entry, with embedded clinical decision support, has great promise in reducing medication errors but preventable adverse drug events may still occur despite such systems.

Objectives:

The purpose of the study was to evaluate whether adding medication profiling (by using a retrospective drug utilization review program) to computerized provider order entry with embedded order checks (drug alerts) reduces the incidence of adverse drug events.

Methods:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
盲法
Single

入排标准

性别
All
接受健康志愿者

入选标准

  • patient must be alive
  • patient must be currently active in GLA system
  • medication for which alert was generated must be currently active
  • patient provider must not be Peter Glassman

排除标准

  • 未提供

研究组 & 干预措施

Arm 1

Other

干预措施: Patient risk profiling (potential ADEs) w/provider feedback (Behavioral)

研究者

申办方类型
Fed
责任方
Sponsor

研究点 (2)

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