Optimization of Transport and Use of a Mobile ECMO Team in Patients With Sudden Cardiac Arrest in the Moravian-Silesian Region

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age3-60
SponsorUniversity Hospital Ostrava

About this trial

This study evaluates the feasibility of implementing a mobile extracorporeal membrane oxygenation (ECMO) team and optimizing patient transport logistics.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

out-of-hospital cardiac arrest

indication for ECPR

Disqualifiers

death at the scene of the accident

withdrawal of the informed consent

Trial population

Patients indicated for ECPR after out-of-hospital cardiac arrest, for whom transport of the patient to an ECMO centre or deployment of an ECMO team is logistically manage-able.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • Extracorporeal cardiopulmonary resuscitation (ECPR)

    Procedure/Surgery

    Extracorporeal cardiopulmonary resuscitation (commonly known as ECPR) is a method of cardiopulmonary resuscitation (CPR) that passes the patient's blood through a machine in a process to oxygenate the blood supply.

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: ECPR and ECMO1 intervention

Trial outcomes

Primary outcomes

1

Neurological outcome after 30 days (CPC score)

Assessment of the neurological status of patients 30 days after the event using the Cerebral Performance Category (CPC) scale, which measures the extent of neurological impairment: * CPC 1 = good neurological condition * CPC 2 = mild impairment * CPC 3-5 = serious impairment, vegetative state or death The primary endpoint of the study is the proportion of patients with a favourable neurological outcome (CPC 1-2).

Time frame
30 days

Secondary outcomes

1

Time from collapse to initiation of ECMO

Measuring the time (in minutes) from patient collapse to ECMO initiation. The aim is to analyse how this time affects neurological outcome.

Time frame
Up to 2 hours
2

Transport time to the ECMO centre

Measurement of the time (in minutes) from the arrival of the Emergency Medical Services (EMS) at the scene to the admission of the patient to the ECMO centre.

Time frame
Up to 2 hours
3

Arrival time for the mobile ECMO team to the scene

Time interval (in minutes) from activation of the mobile ECMO team to its arrival at the scene. The aim is to evaluate the effectiveness of the model and the potential time benefit of intervention in the field.

Time frame
Up to 2 hours

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University Hospital Ostrava

Lead sponsor

Emergency Medical Services, Moravian-Silesian Region

Collaborator