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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03654846
Other study ID # EmergencyEye-POC
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 25, 2018
Est. completion date September 30, 2018

Study information

Verified date October 2018
Source University of Cologne
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Technical advance as broad-bandwidth wireless internet coverage and the ubiquity utilization of smartphones has opened up new possibilities which surpass the normal audio-only telephony. High quality and real-time video-telephony is now feasible. However until now this technology hasn't been deployed in the emergency respond service.

In the hope of helping the detection of the cardiac arrest, offer the possibility to evaluate and correct via a video-instructed CPR (V-CPR) and to facilitate a fast localization of the emergency site, a new software (EmergencyEye®/RAMSES®) was developed which enables the dispatcher a video-telephony with the callers mobile terminal (smartphone) if suitable.

This technology hasn't been tested in a randomized controlled trial in real environment conditions yet. This is to be done in this study.


Description:

Technical advance as broad-bandwidth wireless internet coverage and the ubiquity utilization of smartphones has opened up new possibilities which surpass the normal audio-only telephony. High quality and real-time video-telephony is now feasible. However until now this technology hasn't been deployed in the emergency respond service.

In the hope of helping the detection of the cardiac arrest, offer the possibility to evaluate and correct via a video-instructed CPR (V-CPR) and to facilitate a fast localization of the emergency site, a new software (EmergencyEye®/RAMSES®) was developed which enables the dispatcher a video-telephony with the callers mobile terminal (smartphone) if suitable, and automated localisation of the caller.

This technology hasn't been tested in a randomized controlled trial in real environment conditions yet. This is to be done in this study.


Recruitment information / eligibility

Status Completed
Enrollment 54
Est. completion date September 30, 2018
Est. primary completion date September 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- healthy volunteers

Exclusion Criteria:

- cardiovascular diseases

- pulmonary diseases

- pregnancy

- all other conditions that make CPR impossible

Study Design


Related Conditions & MeSH terms


Intervention

Device:
EmergencyEye
EmergencyEye Smartphone App

Locations

Country Name City State
Germany Department of Anaesthesiology and Critical Care Medicine, University Hospital of Cologne Cologne

Sponsors (1)

Lead Sponsor Collaborator
University of Cologne

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recognition of CPR quality through video transmission Recognition of CPR quality (3 conditions are randomized in each CPR, i.e. Frequency, Compression Depth, Compression Point) in Video-assisted CPR 1 minute of CPR
Secondary Time to first chest compression Time measured from the beginning of the emergency call to the first chest compression Study duration (approx. 1 minute)
Secondary Precision of Geolocalisation Precision of Geolocalisation, i.e. difference between verbally localized and automatically localized (aGPS) respondes to emergency call. Difference in runtimes of dispatched ambulances will be calculated Study duration (approx. 1 minute)
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