跳至主要内容
临床试验/NCT00229671
NCT00229671已完成不适用

Ambulatory Medication Errors and Adverse Drug Events (ADEs) in Pediatrics

Weill Medical College of Cornell University2 个研究点 分布在 1 个国家目标入组 6,341 人开始时间: 2001年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
6,341
试验地点
2
主要终点
Medication Errors

研究概览

简要总结

The purpose of this study is to determine the rates of medication errors in pediatric outpatients in 6 office practices. Further, we wish to determine the effectiveness of a computerized physician order entry (CPOE) system in reducing errors.

详细描述

This study has the following 2 goals:

Aim 1: To determine the rates, types, and predictors of medication errors and ADEs.

Aim 2: To perform a trial assessing the effectiveness of an intervention (CPOE) on reducing serious medication errors.

We hypothesize that:

  1. Medication errors and ADEs are frequent in ambulatory pediatrics.
  2. Presence of the following predictors will be associated with higher error rates: cultural, racial, socioeconomic, educational, and linguistic barriers to communication, understanding, and successful completion of prescribed therapies; complex medical or chronic medical conditions; complex medication regimens; non-physician providers with limited clinical experience; high provider workloads; and complex prescription refill systems.
  3. Prevention strategies, including both technology-based and behavioral/ human factors-based interventions, will be effective and cost-effective in reducing rates of serious medication errors (defined as preventable ADEs and non-intercepted potential ADEs).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
1 Day 至 21 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Pediatric providers at the participating office practices during the study period as well as the parents of the patients of these providers.

排除标准

  • Pediatric providers or patients at other office practices.

结局指标

主要结局

Medication Errors

时间窗: July 2002- August 2003

次要结局

  • Adverse Drug Events(July 2002- August 2003)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验