Ireland
--:--IST
Recruiting Observational

Prehospital ECPR in Moravia Silesia Region

NCT07041086 · tracked via the Priya Life Science Czechia tracker
Phase
Observational
Started
2025-06-17
Last updated
2026-01-15

Condition(s) studied

Cardiac Arrest, Out-Of-Hospital

Investigational drug(s) / intervention(s)

Extracorporeal membrane oxygenation (ECMO)

Extracorporeal membrane oxygenation (ECMO): In extracorporeal membrane oxygenation (ECMO), blood is pumped outside of the body to a heart-lung machine. The machine removes carbon dioxide and sends oxygen-rich blood back to the body. Blood flows from the right side of the heart to the heart-lung machine. It's then rewarmed and sent back to the body.

Study summary

Cardiopulmonary resuscitation (CPR) for out-of-hospital cardiac arrest (OHCA) in specific cases could be improved by Extracorporeal membrane oxygenation (ECMO; ECPR). ECPR could be introduced in hospital after retrieval of an OHCA patient and also faster by implantation on scene. The aim is to verify the effectiveness of ECPR on scene in the Moravian-Silesian region.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 years * Observed collapse and presumption of cardiac cause of cardiac arrest * Estimated age up to 70 years * Baseline rhythm of ventricular fibrillation or pulseless electrical activity (PEA) * Basic bystander cardiopulmonary resuscitation (CPR), "bystander CPR", telephone assisted CPR (TANR) Exclusion Criteria: * Children or adults with estimated weight below 40 kg * Known major comorbidities of the patient suggesting low rehabilitation potential (e.g. chronic obstructive pulmonary disease (COPD) IV, malignancy in tertiary phase)

Primary outcome measure(s)

  • Time from cardiac arrest (collapse) to implantation of ECMO — up to 60 minutes
    The time from cardiac arrest (collapse) to implantation of ECMO will be recorded and assessed
  • Hospital mortality — up to 3 weeks
    Hospital mortality will be assessed for the period of 3 weeks
  • Cerebral Performance Category (CPC) score — 30 days
    Cerebral Performance Category (CPC) score will be observed 30 days after cardiac arrest
  • Neurological outcome (CPC score) — 6 months
    Neurological outcome will be assessed using the Cerebral Performance Category Scale (CPC) 6 months after cardiac arrest.
  • Neurological outcome (SF-36) — 6 months
    Neurological outcome will be assessed using the Short Form 36 Health Subject Questionnaire (SF-36) 6 months after cardiac arrest.
  • Neurological outcome (EQ-5D) — 6 months
    Neurological outcome will be assessed using the European Quality of Life Questionnaire (EQ-5D) 6 months after cardiac arrest.

Trial sites (2)

FacilityCityRegionStatus
Emergency Medical Services, Moravian-Silesian Region Ostrava Moravian-Silesian Region Recruiting
University Hospital Ostrava Ostrava Moravian-Silesian Region Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07041086 on ClinicalTrials.gov ↗ ← All trials in Czechia