Actively Recruiting

Age: 18Years - 70Years
All Genders
ID07041086

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

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

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

Long-term Monitoring

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

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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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