跳至主要内容
临床试验/NCT05994196
NCT05994196已完成不适用

Evaluation of a Patient Prioritization Software for the Secondary Prioritization of Patients in the Pediatric Emergency Department

University Hospital, Lille1 个研究点 分布在 1 个国家目标入组 1,599 人开始时间: 2021年3月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,599
试验地点
1
主要终点
Length of stay

研究概览

简要总结

The goal of this randomized, controlled, open-label trial is to test the use of secondary prioritization software (Optimum®) in the pediatric emergency department (PED).

The aim of this study is to determine:

  1. whether the use of this secondary prioritization software (Optimum®) reduces the patients' median length of stay (LOS) in the PED
  2. how this software is accepted by the staff. The PED staff will be asked to manage the patients according to the Optimum® software indications (intervention) or according to the standard dashboard (control).

详细描述

Design: randomized, controlled open-label trial in the PED at Lille University Medical Center, Lille, France.

Period: between March 15th and April 23rd, 2021.

Randomization: each day was randomized for the use of Optimum® software (intervention group) or the PED's standard patient management dashboard (control group).

Inclusion criteria:

  • All children admitted between 10:00 am and 0:00 am at the PED.

研究设计

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

入排标准

年龄范围
3 Days 至 16 Years(Child)
性别
All
接受健康志愿者

入选标准

  • All children admitted between 10:00 am and 0:00 am

排除标准

  • Patients who left without being seen
  • Patients subsequently admitted to the short-stay unit

结局指标

主要结局

Length of stay

时间窗: from admission to discharge, assessed up to 1 day.

the length of stay for each patient

次要结局

  • Number of patients present(1 day)
  • Pediatric emergency department staff satisfaction(through study completion, an average of 3 months)
  • Time intervals between each stage(1 day)

研究者

发起方
University Hospital, Lille
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

Evaluation of a Software for the Secondary... | 临床试验