Skip to main content
Clinical Trials/NCT01647854
NCT01647854
Completed
Not Applicable

Introduction and Operation of a Mobile Telemedicine System to Support Paramedics in the Emergency Medical Service

RWTH Aachen University1 site in 1 country425 target enrollmentAugust 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prehospital Emergency
Sponsor
RWTH Aachen University
Enrollment
425
Locations
1
Primary Endpoint
Rate of complications
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The aim of the study is to investigate the safety and efficacy of the operation of a prehospital teleconsultation system in the Emergency Medical Service.

Detailed Description

Six ambulances from five different Emergency Medical Service (EMS) districts are equipped with a portable telemedicine system. 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. Also 12-lead-ECGs can be transmitted to the tele-EMS physician. 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 in obtaining all relevant medical history, ECG diagnosis, general diagnosis and can delegate the application of medications. 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. The safety and efficacy of the introduction and operation of this system should be evaluated.

Registry
clinicaltrials.gov
Start Date
August 2012
End Date
May 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • prehospital emergency
  • consent of the patient for teleconsultation was obtained or patient is unable to consent due to the severity of the emergency

Exclusion Criteria

  • patient refuses consent for teleconsultation
  • psychiatric emergency

Outcomes

Primary Outcomes

Rate of complications

Time Frame: up to 2 hours

The incidence of complications due to delegated medications should be evaluated.

Secondary Outcomes

  • Technical assessments(up to 2 hours)
  • Time intervals(up to 2 hours)
  • Duration of teleconsultation(up to 2 hours)
  • Requirement of on-scene EMS physician(up to 2 hours)

Study Sites (1)

Loading locations...

Similar Trials