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Prehospital Emergency Care of Obstructive Respiratory Emergencies With the Use of Teleconsultation

Prehospital Emergency Care of Obstructive Respiratory Emergencies With the Use of Teleconsultation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01644045
Enrollment
17
Registered
2012-07-18
Start date
2012-08-31
Completion date
2015-09-30
Last updated
2015-09-22

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

Conditions

Asthma, COPD

Keywords

Asthma, COPD, emergency medical service, teleconsultation, telemedicine

Brief summary

The aim of the study is to investigate the quality of prehospital emergency care in acute respiratory emergencies, when paramedics are supported telemedically by an EMS physician.

Detailed description

Six ambulances from five different Emergency Medical Service (EMS) districts are equipped with a portable telemedicine system. In cases of acute obstructive, respiratory emergencies the paramedics can use this system to contact a so called tele-EMS physician after consent of the patient was 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), 12-lead-ECGs and video streaming from the inside of the ambulance can also be carried out, if indicated. The tele-EMS physician supports the EMS team in obtaining all relevant medical history, 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 quality of prehospital care and the possible influences on the initial inhospital phase should be investigated and compared with regular EMS.

Interventions

DEVICETeleconsultation

Teleconsultation for the EMS in acute respiratory emergencies

Sponsors

RWTH Aachen University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Obstructive, respiratory emergency * Verbal consent for teleconsultation obtained or patient is not able to consent due the severity of the emergency

Exclusion criteria

* No respiratory emergency * Refused consent for teleconsultation

Design outcomes

Primary

MeasureTime frameDescription
Oxygen Saturationaverage 1 hourMeasurement of pulse oximetric oxygen saturation at the timepoint of first contact with a physician (EMS physician OR hospital arrival)

Secondary

MeasureTime frameDescription
Quality of emergency careaverage 1 hourAnalysis of the quality of prehospital care on the basis of published guidelines for asthma / COPD.
Rate of ventilationaverage 1 hourFraction of patients that receive invasive or non-invasive ventilation during the prehospital phase
Rate of complications2 hoursRate of complications due to medications: allergic reaction, heart rhythm problems

Countries

Germany

Outcome results

None listed

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