NCT07374289

Brief Summary

On-scene extracorporeal pulmonary resuscitation (ECPR) for out-of-hospital cardiac arrest (OHCA) seems to speed up the start of extracorporeal membrane oxygenation (ECMO) and shorten low flow during cardiopulmonary resuscitation (CPR) in case of refractory cardiac arrest. The primary goal is to verify the benefit of on-scene ECPR in terms of shortening the collapse-to-ECMO interval. The secondary goal is to compare outcomes in the on-scene ECPR group with hospital cannulation.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
90

participants targeted

Target at P50-P75 for not_applicable

Timeline
45mo left

Started Jan 2026

Longer than P75 for not_applicable

Geographic Reach
1 country

2 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress7%
Jan 2026Dec 2029

First Submitted

Initial submission to the registry

January 9, 2026

Completed
19 days until next milestone

First Posted

Study publicly available on registry

January 28, 2026

Completed
2 days until next milestone

Study Start

First participant enrolled

January 30, 2026

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2028

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2029

Last Updated

January 30, 2026

Status Verified

January 1, 2026

Enrollment Period

2.9 years

First QC Date

January 9, 2026

Last Update Submit

January 28, 2026

Conditions

Keywords

extracorporeal membrane oxygenationout-of-hospital cardiac arrestcardiac arrestcardiogenic shock

Outcome Measures

Primary Outcomes (3)

  • Hospital survival

    Hospital survival will be assessed 30 days after the cardiac arrest

    30 days after the cardiac arrest

  • ICU stay

    The length of the Intensive Care Unit (ICU) stay will be assessed in days.

    Through the ICU stay, on average 12 days

  • Neurologic outcomes

    Neurologic outcomes will be assessed in patients using the Cerebral Performance Category (CPC) score. The CPC score is a 1-to-5 scale assessing neurological outcome, most commonly after cardiac arrest, where 1 is best (normal brain function) and 5 is worst (brain death).

    30 days after the cardiac arrest

Secondary Outcomes (4)

  • Collapse to ECMO interval

    One hour

  • Collapse to ECMO interval

    From the collapse (cardiac arrest) to ECMO initiation

  • Long-term outcome - Survival

    6 months after the collapse

  • Long-term outcome - Quality of Life

    6 months after the collapse

Study Arms (2)

ECPR on scene

EXPERIMENTAL

On-scene ECPR cannulation by mobile ECMO team according to protocol if the location of the arrest and circumstances appear to be suitable (distance from the ECMO centre, transport logistics, in an ambulance/at home, etc.)

Procedure: Prehospital ECMO cannulation on scene of cardiac arrest

ECPR in hospital

ACTIVE COMPARATOR

Hospital ECPR cannulation at Emergency Department by ECMO team accord-ing to protocol if a on scene ECPR call-out was not indicated.

Procedure: Transfer with ongoing mechanical chest compression to hospital followed by hospital ECMO cannulation

Interventions

ECPR (Extracorporeal Cardiopulmonary Resuscitation) is a critical, advanced resuscitation technique using Veno-arterial Extracorporeal Membrane Oxygenation for patients in cardiac arrest where conventional CPR fails, functioning as a bridge to restore circulation and oxygenation by pumping and oxygenating blood outside the body before returning it.

ECPR on scene

ECPR (Extracorporeal Cardiopulmonary Resuscitation) is a critical, advanced resuscitation technique using Veno-arterial Extracorporeal Membrane Oxygenation for patients in cardiac arrest where conventional CPR fails, functioning as a bridge to restore circulation and oxygenation by pumping and oxygenating blood outside the body before returning it.

ECPR in hospital

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Presumed cardiac aetiology of the cardiac arrest
  • Witnessed collapse
  • Bystander CPR
  • Estimated age ≤ 70 years
  • Body weight ≥15 Kg

You may not qualify if:

  • Known terminal malignant disease
  • Known terminal chronic disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Emergency Medical Services, Moravian-Silesian Region

Ostrava, Moravian-Silesian Region, 700 30, Czechia

RECRUITING

University Hospital Ostrava

Ostrava, Moravian-Silesian Region, 708 52, Czechia

RECRUITING

MeSH Terms

Conditions

Heart ArrestShock, CardiogenicOut-of-Hospital Cardiac Arrest

Interventions

Parturition

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular DiseasesMyocardial InfarctionMyocardial IschemiaVascular DiseasesInfarctionIschemiaPathologic ProcessesPathological Conditions, Signs and SymptomsNecrosisShock

Intervention Hierarchy (Ancestors)

PregnancyReproductionReproductive Physiological PhenomenaReproductive and Urinary Physiological Phenomena

Study Officials

  • Filip Burša, MD, PhD, EDEC

    University Hospital Ostrava

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Jiří Hynčica

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Masking Details
No masking will be used in the study.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: The study subjects will be enrolled in two parallel arms
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 9, 2026

First Posted

January 28, 2026

Study Start

January 30, 2026

Primary Completion (Estimated)

December 31, 2028

Study Completion (Estimated)

December 31, 2029

Last Updated

January 30, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

There is no plan to make individual participant data available to other researchers. The data may be provided upon reasonable request.

Locations