Prehospital ECPR in Moravia Silesia Region
Condition(s) studied
Investigational drug(s) / intervention(s)
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| Emergency Medical Services, Moravian-Silesian Region | Ostrava | Moravian-Silesian Region | Recruiting |
| University Hospital Ostrava | Ostrava | Moravian-Silesian Region | Recruiting |
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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