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Operation of a Mobile Telemedicine System in the EMS

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01647854
Enrollment
425
Registered
2012-07-24
Start date
2012-08-31
Completion date
2015-05-31
Last updated
2015-09-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prehospital Emergency, Safety, Teleconsultation

Keywords

emergency medical service, telemedicine, teleconsultation, safety

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.

Interventions

PROCEDURETeleconsultation

Teleconsultation in prehospital emergencies

Sponsors

RWTH Aachen University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Rate of complicationsup to 2 hoursThe incidence of complications due to delegated medications should be evaluated.

Secondary

MeasureTime frameDescription
Time intervalsup to 2 hourson-scene time of EMS, contact (EMS) to hospital arrival time
Duration of teleconsultationup to 2 hoursAnalysis of the time requirement for teleconsultation with respect to the different EMS districts and different emergencies as well as over time.
Requirement of on-scene EMS physicianup to 2 hoursAnalysis of the requirement of an on-scene EMS physician in respect to the different emergencies and districts.
Technical assessmentsup to 2 hoursAnalysis of the technical performance of the system

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026