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RecruitingNCT07374289Updated Jan 30, 2026

On Scene ECPR in Ostrava

An interventional study of Prehospital ECMO cannulation on scene of cardiac arrest and Transfer with ongoing mechanical chest compression to hospital followed by hospital ECMO cannulation in Cardiac Arrest (CA) and Cardiogenic Shock, sponsored by University Hospital Ostrava. Recruiting at 2 sites in Czechia. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-01-30.

Sponsored by University Hospital Ostrava · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Non-randomized
Ages
18 Years to 70 Years
Sex
All
01

Study 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.

Read the detailed description

ECPR is a life-saving method for a selected group of patients who are refractory to standard resuscitation procedures. With the appropriate use of ECPR, it is possible to achieve a significant improvement in survival with good neurological outcomes even in patients who would otherwise die. The ECMO Centre Ostrava has been providing ECPR for OHCA since 2022 with cannulation in the hospital after prior transport from the scene under continuous resuscitation. A good neurological outcome is achieved in approximately 29% of patients, even though the collapse-ECMO interval is around 75 minutes. Shortening this interval, which is associated with improved outcomes, is possible by using a mobile team that per-forms cannulation directly on scene. Mobile ECPR will be carried out in cooperation with the Ostrava University Hospital and the Moravian-Silesian Region Emergency Medical Service. The primary objective is to verify the benefit of on-scene ECPR in terms of shortening the collapse-ECMO interval. The secondary objective is to compare the outcome in the on-scene ECPR group with hospital cannulation.

02

Conditions studied

  • Cardiac Arrest (CA)
  • Cardiogenic Shock

Keywords

  • extracorporeal membrane oxygenation
  • out-of-hospital cardiac arrest
  • cardiac arrest
  • cardiogenic shock
03

In context

Heart Arrest

926 studies on the registry are indexed under Heart Arrest; 226 are open to participants now.

This study's planned enrollment of 90 is close to the median of 100 across 518 interventional studies indexed under Heart Arrest.

Browse Heart Arrest studies →

Lead sponsor

University Hospital Ostrava is the lead sponsor of 148 studies on the registry; 50 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • Known terminal malignant disease
  • Known terminal chronic disease
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
90 participants (estimated)

Study arms

  • Experimental
    ECPR on scene

    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

  • Active comparator
    ECPR in hospital

    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

  • ProcedurePrehospital ECMO cannulation on scene of cardiac arrest

    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.

  • ProcedureTransfer with ongoing mechanical chest compression to hospital followed by hospital ECMO cannulation

    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.

06

What researchers measure

Primary outcomes

  1. Hospital survival

    Hospital survival will be assessed 30 days after the cardiac arrest

    Time frame: 30 days after the cardiac arrest

  2. ICU stay

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

    Time frame: Through the ICU stay, on average 12 days

  3. 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).

    Time frame: 30 days after the cardiac arrest

Secondary outcomes

  1. Collapse to ECMO interval

    The interval from the collapse (cardiac arrest) to ECMO initiation will be measured in minutes.

    Time frame: One hour

  2. Collapse to ECMO interval

    The interval from the collapse (cardiac arrest) to ECMO initiation will be measured in minutes.

    Time frame: From the collapse (cardiac arrest) to ECMO initiation

  3. Long-term outcome - Survival

    The long-term survival of patients will be assessed 6 months after the collapse.

    Time frame: 6 months after the collapse

  4. Long-term outcome - Quality of Life

    Long-term quality of life will be assessed 6 months after the collapse using standardised tools (questionnaires).

    Time frame: 6 months after the collapse

07

Study locations

2 of 2 sites recruiting
  • Emergency Medical Services, Moravian-Silesian Region
    Ostrava, Moravian-Silesian Region 700 30, Czechia
    Recruiting
    • David Holeš, MD, PhD · Contactzzsmsk@zzsmsk.cz · +42059701
    • David Holeš, MD, PhD · Principal investigator
  • University Hospital Ostrava
    Ostrava, Moravian-Silesian Region 708 52, Czechia
    Recruiting
    • Jiří Hynčica · Contactjiri.hyncica@fno.cz · +42059737
    • Filip Burša, MD, PhD, EDEC · Principal investigator
08

References and documents

Individual participant data

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

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Jan 2026; primary completion for Dec 2028, 35 months later.

Of 204 non-industry interventional studies with no phase under Heart Arrest, half reached primary completion within 29 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 47. This study's planned 35 months is above that.

Counting every sponsor, half of 218 studies reached it within 28 months; a quarter within 10 and three quarters within 47.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 9, 2026
First posted
Jan 28, 2026
StartEst.
Jan 30, 2026
Primary completionEst.
Dec 31, 2028
CompletionEst.
Dec 31, 2029
Last update
Jan 30, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jan 30, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07374289
Collaborators
Emergency Medical Services, Moravian-Silesian Region
Responsible party
Sponsor
First posted
Jan 28, 2026
Start date
Jan 30, 2026 (estimated)
Primary completion
Dec 31, 2028 (estimated)
Completion
Dec 31, 2029 (estimated)
Last update
Jan 30, 2026

Study contacts

Jiří Hynčica
Contact
jiri.hyncica@fno.cz
+42059737 ext. 2587
Filip Burša, MD, PhD, EDEC
principal investigator · University Hospital Ostrava

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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