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Wroclaw Out-Of-Hospital Cardiac Arrest Registry

Wroclaw Out-Of-Hospital Cardiac Arrest Registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05132387
Acronym
WOHCA
Enrollment
50
Registered
2021-11-24
Start date
2021-10-25
Completion date
2028-01-01
Last updated
2025-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Out-Of-Hospital Cardiac Arrest

Keywords

Cardiac arrest, ECMO, ECMO-CPR

Brief summary

The purpose of this study is to assess the efficacy of institutionalized care program of patients with out-of-hospital cardiac arrest.

Detailed description

Patients with out-of-hospital cardiac arrest included in the program will be treated with extracorporeal membrane oxygenation (ECMO) assisted cardiopulmonary resuscitation (CPR) with additional invasive procedures including coronary/pulmonary angiography and intervention. This type of treatment was not provided in institutionalized fashion in Wroclaw, Poland. Implementation of this program should improve survival in out-of-hospital cardiac arrest patients, which currently is less than 10%.

Interventions

OTHERECMO assisted CPR in out-of-hospital cardiac arrest

Patients included in the registry will be transferred during LUCAS assisted CPR by the Wroclaw Emergency Medical Services to the Emergency Department of the Wroclaw University Hospital where blood gasses will be assessed. If two or more of the following: end-tidal carbon dioxide (CO2) \> 10 mm Hg, arterial partial pressure of oxygen (PaO2) \>50 mm Hg or oxygen saturation \>85%, and lactic acid \<18 mmol/L will be fulfilled patient will be further transferred to the Cardiac Catheterization Laboratory for V-A ECMO implantation followed by coronary/pulmonary artery angiography and intervention.

Sponsors

Wroclaw Emergency Medical Services
CollaboratorUNKNOWN
Wroclaw Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Age \< 60 years * witnessed sudden cardiac arrest with immediate CPR * supposed cardiac cause of the event * ventricular fibrillation (VF) or pulseless ventricular tachycardia (VT) at first medical contact with 3 unsuccessful defibrillations (no ROSC) * CPR conducted with Lund University Cardiopulmonary Assist System (LUCAS™) * Estimated transfer time from the scene to the Emergency Department \< 30 minutes. * End tidal carbon dioxide (ETCO2) \> 10 mmHg

Exclusion criteria

* Total presumed time from 112 call to ECMO implantation longer than 60 minutes * Age \< 18 years old or \> 60 years old; * Non-shockable initial rhythm * Unavailability of the automated CPR device * Unavailability of the catheterisation laboratory * Severe concomitant illness with decreased life expectancy * Severe body injury * Severe active bleeding * Drowning * Terminal cancer

Design outcomes

Primary

MeasureTime frameDescription
mortality1 monthall cause mortality

Secondary

MeasureTime frameDescription
degree of disability3 and 6 months after index eventModified Rankin Scale of 3 or lower

Countries

Poland

Contacts

Primary ContactWiktor Kuliczkowski, MD
wiktor.kuliczkowski@umw.edu.pl+ 48 603 707 093

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026