跳至主要内容
临床试验/NCT01644032
NCT01644032已完成不适用

Telemedically Supported Analgesia in the Emergency Medical Service

RWTH Aachen University2 个研究点 分布在 1 个国家目标入组 106 人开始时间: 2012年8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
106
试验地点
2
主要终点
Rate of complications

研究概览

简要总结

The aim of the study is to evaluate the safety and efficacy of telemedically supported and delegated pain therapy in the Emergency Medical Service (EMS).

详细描述

Six ambulances from five different Emergency Medical Service (EMS) districts are equipped with a portable telemedicine system. In cases of emergencies, where intravenous analgesia is necessary, the paramedics can use this system to contact a so called "tele-EMS physician" after consent of the patient is obtained. The tele-EMS physician has an audio-connection to the EMS team and receives vital parameters (e.g., ECG, pulse oximetry, non-invasive blood pressure) in real-time. The transmission of still pictures - taken with a smartphone - and video streaming from the inside of the ambulance can be carried out, if meaningful. The tele-EMS physician supports the EMS team and can delegate the application of morphine and other analgesics. This can be carried out to bridge the time to the arrival of an EMS physician or in less severe cases without an EMS physician on-scene.

All regular ambulances of the five districts are not allowed to administer analgesics without an physician on-scene. They have to call an Advanced Life Support response unit, staffed with an EMS physician, who carries out all kinds of ALS interventions.

The safety, efficacy and the quality of analgesia should be compared with regular EMS.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Verbal consent obtained or patient is unable to consent due to the severity of the emergency
  • Indication for analgesia

排除标准

  • Refused consent
  • No indication for analgesia

结局指标

主要结局

Rate of complications

时间窗: 2 hours

Definition of complications: respiratory insufficiency, allergic reaction, circulatory insufficiency

次要结局

  • Time intervals(average 1 hour)
  • Medications and dosages(average 1 hour)
  • Pain level(average 1 hour)
  • Incidence of nausea and vomiting(2 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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