NCT07679737

Brief Summary

CHEER4TTE is a target trial emulation, designed to simulate a randomised controlled trial by utilising data from pre-existing data sources. The aim is to determine whether prehospital ECPR for refractory out-of-hospital cardiac arrest improves the rate of survival to hospital discharge when compared to conventional cardiac arrest care.

Trial Health

75
On Track

Trial Health Score

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

Enrollment
250

participants targeted

Target at P75+ for all trials

Timeline
2mo left

Started Jan 2025

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress90%
Jan 2025Oct 2026

Study Start

First participant enrolled

January 1, 2025

Completed
1.4 years until next milestone

First Submitted

Initial submission to the registry

June 9, 2026

Completed
22 days until next milestone

First Posted

Study publicly available on registry

July 1, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2026

Last Updated

July 1, 2026

Status Verified

June 1, 2026

Enrollment Period

1.7 years

First QC Date

June 9, 2026

Last Update Submit

June 30, 2026

Conditions

Keywords

ECMOECPRExtracorporeal membrane oxygenationECMO CPRat the scenescene basedOHCA

Outcome Measures

Primary Outcomes (1)

  • Survival to hospital discharge

    From meeting full eligibility criteria until the date/time of death or hospital discharge, assessed up to 180 days

Secondary Outcomes (5)

  • Low flow time

    time from onset of arrest to time of ECPR flow, or time of death

  • ICU length of stay

    From the date/time of ICU admission until the date/time of ICU discharge/death, assessed up to 180 days

  • Mechanical ventilation days

    From date/time of mechanical ventilation commencement until date/time of liberation from mechanical ventilation assessed up to 180 days

  • ECMO complications

    From the date/time of commencement of ECMO support until 1 week following the date/time of cessation of ECMO support

  • Rates of organ and tissue donation in non-survivors

    In the 48hours following date/time of death

Study Arms (2)

Prehospital Extracorporeal Cardiopulmonary Resuscitation (ECPR) Strategy

Patients with refractory OHCA treated with scene-based, pre-hospital ECPR (Intervention) will be identified within two studies testing feasibility of prehospital ECPR for refractory OHCA in the metropolitan regions of Melbourne and Sydney. All intra-arrest and post-arrest care follow guidelines based on the Australian and New Zealand Council of Resuscitation recommendations supplemented by the Victorian ECMO Service (VECMOS) guidelines within Victoria and Agency for Clinical Innovation ECMO Clinical Practice Guidelines in NSW.

Other: Extracorporeal cardiopulmonary resuscitation

Conventional Cardiac Arrest Strategy

Patients with refractory OHCA treated with conventional cardiac arrest strategy (standard care) will be identified within NSW and Victorian Ambulance OHCA Registries. All intra-arrest and post-arrest care for patients in this group follow guidelines based on the Australian and New Zealand Council of Resuscitation recommendations.

Interventions

The Intervention being evaluated is the initiation of extracorporeal cardiopulmonary resuscitation (ECPR) at the scene, in addition to conventional cardiac arrest care.

Also known as: Extracorporeal Cardiopulmonary Resuscitation (ECPR), Prehospital ECPR, Scene based ECPR
Prehospital Extracorporeal Cardiopulmonary Resuscitation (ECPR) Strategy

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adult patients with refractory out-of-hospital cardiac arrest in the metropolitan regions of Sydney and Melbourne.

You may qualify if:

  • Witnessed cardiac arrest
  • Bystander CPR
  • Refractory cardiac arrest (failure to achieve sustained ROSC \>20 minutes)
  • Initial cardiac rhythm VF, VT or PEA
  • Within the hours of prehospital ECPR service operation

You may not qualify if:

  • Initial cardiac rhythm asystole
  • ROSC with sustained recovery
  • Unable to reach the patient and commence cannulation within 45 minutes of onset of arrest
  • Evidence of/suspected end-stage disease:
  • severe disability impairing activities of daily living
  • end-stage organ disease - cardiac, liver, lung, renal
  • other life-limiting diseases, e.g. malignancy, terminal illness
  • advance health care directive
  • Time periods of advanced public health restrictions in Victoria and NSW due to COVID-19

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Monash University

Melbourne, Victoria, Australia

Location

MeSH Terms

Conditions

Out-of-Hospital Cardiac Arrest

Condition Hierarchy (Ancestors)

Heart ArrestHeart DiseasesCardiovascular Diseases

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 9, 2026

First Posted

July 1, 2026

Study Start

January 1, 2025

Primary Completion (Estimated)

October 1, 2026

Study Completion (Estimated)

October 1, 2026

Last Updated

July 1, 2026

Record last verified: 2026-06

Locations