Actively Recruiting
Prehospital ECPR in Moravia Silesia Region - Assessing the Effectiveness, Feasibility and Timing of ECMO for Out-of-Hospital Cardiac Arrest
Led by University Hospital Ostrava · Updated on 2026-01-15
100
Participants Needed
2
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University Hospital Ostrava
Lead Sponsor
E
Emergency Medical Services, Moravian-Silesian Region
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the use of Extracorporeal Membrane Oxygenation (ECMO), also called ECPR, during cardiopulmonary resuscitation (CPR) for patients who experience out-of-hospital cardiac arrest (OHCA). The study aims to determine if starting ECMO treatment directly at the scene of the cardiac arrest, rather than after hospital arrival, can improve neurological outcomes and survival in the Moravian-Silesian region. This observational study explores the feasibility and effectiveness of this approach compared to standard hospital-based ECMO initiation. The intervention involves connecting suitable OHCA patients to ECMO on site by a specialized ECMO team working alongside emergency medical services. ECMO supports the heart and lungs by pumping blood through an external machine that oxygenates and warms it before returning it to the body. The study focuses on patients with ventricular fibrillation or pulseless electrical activity rhythms who receive bystander CPR and are estimated to be between 18 and 70 years old. The ECMO team is dispatched simultaneously with the ambulance to shorten the time from collapse to ECMO initiation. Participants will be monitored from the time of cardiac arrest through hospital treatment and follow-up periods up to six months. Key measures include the time to ECMO implantation, hospital mortality within three weeks, and neurological outcomes assessed by Cerebral Performance Category (CPC) scores and quality of life tools (SF-36 and EQ-5D) at 30 days and six months. The study also simulates emergency scenarios to validate the logistics and timing of on-scene ECMO application. This research will help establish if early ECMO in the field can improve recovery chances after cardiac arrest.
CONDITIONS
Brief Title
Prehospital ECPR in Moravia Silesia Region
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Witnessed collapse with presumed cardiac cause of cardiac arrest
- Estimated age up to 70 years
- Baseline rhythm of ventricular fibrillation or pulseless electrical activity (PEA)
- Received basic bystander cardiopulmonary resuscitation (CPR), including telephone-assisted CPR
You will not qualify if you...
- Children or adults with estimated weight below 40 kg
- Known major comorbidities indicating low rehabilitation potential, such as severe chronic obstructive pulmonary disease (COPD) stage IV or advanced cancer
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 3 weeks
Participants who experience out-of-hospital cardiac arrest and receive extracorporeal membrane oxygenation (ECMO) are observed in the field and hospital to assess the timing and effectiveness of ECMO.
Hospital monitoring visits until discharge or up to 3 weeks
Duration - 6 months
Participants are followed for neurological outcome assessments including Cerebral Performance Category score and quality of life measures.
Follow-up visits for neurological assessments
Trial Site Locations
Total: 2 locations
1
Emergency Medical Services, Moravian-Silesian Region
Ostrava, Moravian-Silesian Region, Czechia, 700 30
Actively Recruiting
2
University Hospital Ostrava
Ostrava, Moravian-Silesian Region, Czechia, 70852
Actively Recruiting
Research Team
J
Jiří Hynčica
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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