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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05132387
Other study ID # 327/2021
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 25, 2021
Est. completion date January 1, 2025

Study information

Verified date June 2024
Source Wroclaw Medical University
Contact Wiktor Kuliczkowski, MD
Phone + 48 603 707 093
Email wiktor.kuliczkowski@umw.edu.pl
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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


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%.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date January 1, 2025
Est. primary completion date October 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
ECMO 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.

Locations

Country Name City State
Poland Wroclaw University Hostpital Wroclaw

Sponsors (2)

Lead Sponsor Collaborator
Wroclaw Medical University Wroclaw Emergency Medical Services

Country where clinical trial is conducted

Poland, 

References & Publications (2)

Sip M, Puslecki M, Klosiewicz T, Zalewski R, Dabrowski M, Ligowski M, Goszczynska E, Paprocki C, Grygier M, Lesiak M, Jemielity M, Perek B. A concept for the development of a pioneer regional Out-of-Hospital Cardiac Arrest Program to improve patient outcomes. Kardiol Pol. 2020 Sep 25;78(9):875-881. doi: 10.33963/KP.15433. Epub 2020 Jun 16. — View Citation

Yannopoulos D, Bartos J, Raveendran G, Walser E, Connett J, Murray TA, Collins G, Zhang L, Kalra R, Kosmopoulos M, John R, Shaffer A, Frascone RJ, Wesley K, Conterato M, Biros M, Tolar J, Aufderheide TP. Advanced reperfusion strategies for patients with out-of-hospital cardiac arrest and refractory ventricular fibrillation (ARREST): a phase 2, single centre, open-label, randomised controlled trial. Lancet. 2020 Dec 5;396(10265):1807-1816. doi: 10.1016/S0140-6736(20)32338-2. Epub 2020 Nov 13. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary mortality all cause mortality 1 month
Secondary degree of disability Modified Rankin Scale of 3 or lower 3 and 6 months after index event
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