跳至主要内容
临床试验/NCT02365792
NCT02365792撤回不适用

Efficacy of a Clinical Decision Support System in Prehospital Care: Single Blind, Randomized Clinical Trial.

KU Leuven2 个研究点 分布在 1 个国家开始时间: 2016年6月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
发起方
KU Leuven
试验地点
2
主要终点
Treatment protocol adherence

研究概览

简要总结

The ProDEms-trial focuses on nurses and ambulance drivers working in prehospital care, taking care on the one hand of patients suffering from time-sensitive critical conditions like STEMI, acute stroke or severe traumatic brain injury, and on the other hand of patients whose lives are not in immediate danger but suffer from acute exacerbation of chronic conditions or suffer from acute pain.

In the current study the investigators will use a multistage approach to test the hypothesis whether the use of a CDSS in prehospital emergency care will: 1. Improve protocol adherence, 2. Reduce emergency department length of stay, 3. Improves diagnostic accuracy; without impeding the workflow of the prehospital team or impairing patient safety.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Health Services Research
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
1 Year 至 112 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients who receive treatment from the Paramedic Intervention Team (PIT) in the prehospital Emergency Medical Services (EMS) area of the University Hospitals, Leuven.

排除标准

  • Patient-related interventions not dispatched by the Emergency Medical Dispatch center (EMD)
  • Patient related interventions during transport between two healthcare facilities or in mass casualty situations.

结局指标

主要结局

Treatment protocol adherence

时间窗: Up to 12 months

Measured by comparing the prescribed actions to be taken following the selected standing order (-s) or procedures, with the actual action (-s) taken.

次要结局

  • Alignment between diagnostic accuracy and interventions taken.(Up to 12 months)
  • Length of Stay in the ED(Up to 12 months)
  • Prehospital Patient Time Interval(Up to 12 months)
  • Consistency in reported diagnose and the choice of PIT standing order (-s) or procedure (-s)(Up to 12 months)

研究者

发起方
KU Leuven
申办方类型
Other
责任方
Principal Investigator
主要研究者

Olivier Hoogmartens

Head of the Academic Center for General Practice

KU Leuven

研究点 (2)

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