Clinical trial Recruiting at 1 site Interventional Ages 18 to 70

Prehospital access to extracorporeal cardiopulmonary resuscitation in Prague

Official title: Prehospital Extracorporeal Cardiopulmonary Resuscitation: A Pilot Study in Prague

Run by General University Hospital, Prague · NCT06789978 · Data updated 2026-11-12

This study is testing if a special emergency treatment called prehospital extracorporeal cardiopulmonary resuscitation (ECPR) can help people who have a cardiac arrest outside of the hospital survive better and have better brain function compared to those who only get treatment in the hospital.

More Out-Of-Hospital Cardiac Arrest trials

Quick facts

Study typeInterventional
Ages18 Years to 70 Years
SexAll
Enrollment20 (estimated)
SponsorGeneral University Hospital, Prague
Academic / other
Locations1 site (Prague, Czechia)
StatusRecruiting
StartedJanuary 20, 2025
Main results expectedJune 16, 2026
Study endsJune 16, 2026
Registry record updatedFebruary 14, 2025
Trial IDNCT06789978 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 18-70 who have experienced a witnessed refractory out-of-hospital cardiac arrest.

Probably not a fit

Patients who may not benefit from this study include those with unwitnessed cardiac arrest, asystole, or known severe neurological impairment prior to the event.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This pilot feasibility study aims to evaluate the effectiveness of a prehospital extracorporeal cardiopulmonary resuscitation (ECPR) system for patients experiencing refractory out-of-hospital cardiac arrest (OHCA) in Prague. The study will compare outcomes of patients receiving prehospital ECPR to a historical cohort of those who received in-hospital ECPR. The intervention involves deploying an ECPR team to provide advanced resuscitation techniques in the field. The study seeks to determine if this approach can improve survival rates and neurological outcomes for patients in critical condition.

Why it matters

Potential benefit: If successful, this approach could significantly improve survival rates and neurological outcomes for patients experiencing cardiac arrest outside of a hospital setting.

How similar studies have gone: While the concept of prehospital ECPR is emerging, this specific approach is novel and has not been extensively tested in prior studies.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Estimated age 18-70 years
* Refractory out-of-hospital cardiac arrest (3 unsuccessful defibrillations and/or at least 10 minutes of resuscitation in case of pulseless electrical activity)
* Witnessed cardiac arrest
* ECPR team available
* ECPR team alert within 20 minutes from the emergency call

Exclusion Criteria:

* Unwitnessed cardiac arrest
* Asystole
* ETCO2 less than 10 mmHg upon ECPR team arrival
* Known limitations of intensive care (Do Not Resuscitate - DNR status)
* Known severe neurological impairment prior to cardiac arrest (mRS 4-6)
* Suspected or known pregnancy

Where it's running

  • General University Hospital in Prague
    Prague, Czechia, Czechia
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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  • Super-Early Neuroprognostication in eCPR Patients

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  • Early double sequential defibrillation for cardiac arrest outside the hospital

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.