Optimization of Transport and Use of a Mobile ECMO Team in Patients With Sudden Cardiac Arrest in the Moravian-Silesian Region
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Extracorporeal cardiopulmonary resuscitation (ECPR).
- Who it may be relevant to
- Registry conditions: Cardiac Arrest With Successful Resuscitation, Cardiac Arrest, Cause Unspecified. Basic parameters: 3 years — 60 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Czechia
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Proposal for the Organisation of the Procedure for Extracorporeal Cardiopulmonary Resuscitation of Patients With Sudden Cardiac Arrest in the Pre-hospital Environment of the Moravian-Silesian Region
Overview
This study evaluates the feasibility of implementing a mobile extracorporeal membrane oxygenation (ECMO) team and optimizing patient transport logistics.
Detailed description
The aim of the study is to improve neurological outcomes in out-of-hospital cardiac arrest (OHCA) cases in the Moravian-Silesian Region. By analysing regional epidemiological and demographic data, the project aims to identify key factors for reducing the time from collapse to the initiation of ECMO and to support the development of effective protocols for extracorporeal cardiopulmonary resuscitation (ECPR).
Interventions
- Procedure Extracorporeal cardiopulmonary resuscitation (ECPR)
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.
Primary outcome measures
- Neurological outcome after 30 days (CPC score) [Time frame: 30 days]
Secondary outcome measures (3)
- Time from collapse to initiation of ECMO [Time frame: Up to 2 hours]
- Transport time to the ECMO centre [Time frame: Up to 2 hours]
- Arrival time for the mobile ECMO team to the scene [Time frame: Up to 2 hours]
Eligibility criteria
Inclusion criteria
- out-of-hospital cardiac arrest
- indication for ECPR
Exclusion criteria
- death at the scene of the accident
- withdrawal of the informed consent
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-only
Study locations
Czechia · 2 centers
- Emergency Medial Services, Moravian-Silesian Region — Ostrava
- University Hospital Ostrava — Ostrava
Identifiers
NCT: NCT07009652 · CEPR-01-ECPR