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Prehospital Telemedical Support in Acute Stroke

Prehospital Telemedical Support in Acute Stroke

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01644019
Enrollment
28
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

Acute Stroke

Keywords

stroke, teleconsultation, telemedicine, emergency medical service

Brief summary

The aim of the study is to investigate the quality of prehospital emergency care in acute stroke, 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 suspected acute stroke (including intracranial hemorrhage), 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), 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, neurological 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 quality of prehospital care and the possible influences on the initial inhospital phase should be investigated and compared with regular EMS.

Interventions

PROCEDURETeleconsultation

Teleconsultation of an EMS physician in cases of suspected acute stroke

Sponsors

RWTH Aachen University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* suspected acute stroke * verbal consent for teleconsultation obtained or patient is not able to consent due to the severity of the emergency

Exclusion criteria

* no suspected stroke * patient refuses consent

Design outcomes

Primary

MeasureTime frameDescription
Quality of prehospital careaverage 1 hourAnalysis of the quality of prehospital care on the basis of published guidelines for acute stroke

Secondary

MeasureTime frameDescription
Clinical time intervals12 hoursPrehospital and in-hospital time intervals: on-scene-time, contact to hospital time, door (hospital) to cerebral imaging, door (hospital) to thrombolysis
Diagnostic qualityup to 28 daysComparison of prehospital and definitive diagnosis
Information transfer2 hoursAmount of stroke specific information that is transferred to the admitting hospital.
choice of appropriate hospitalaverage 1 hourEvaluation how many patients are transported to an appropriate facility (stroke unit)

Countries

Germany

Outcome results

None listed

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