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Emergency Resuscitative Endovascular Balloon Occlusion of the Aorta in Out of Hospital Cardiac Arrest

NCT06071910 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2026-03-02

No results posted yet for this study

Summary

This study will assess the feasibility of performing pre-hospital resuscitative endovascular balloon occlusion of the aorta (REBOA) as an adjunct to conventional Advanced Life Support (ALS) in patients suffering from non-traumatic out of hospital cardiac arrest (OHCA). As well as providing valuable insights into the technical feasibility of performing this procedure as part of a resuscitation attempt, the study will also document the beneficial physiological effects of REBOA in this group of patients.

Conditions

  • Out-Of-Hospital Cardiac Arrest
  • Cardiac Arrest
  • Cardiac Arrhythmia
  • Ventricular Fibrillation
  • Ventricular Arrythmia
  • Pulseless Electrical Activity

Interventions

DEVICE

ER-REBOA catheter

To achieve rapid aortic occlusion

Sponsors & Collaborators

  • East Anglian Air Ambulance

    collaborator UNKNOWN

  • Rosetrees Trust

    collaborator OTHER

  • The Dowager Countess Eleanor Peel Trust

    collaborator UNKNOWN

  • The Drummond Foundation

    collaborator UNKNOWN

  • Queen Mary University of London

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-04
Primary Completion
2026-06-01
Completion
2026-12-31
FDA Device
Yes

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06071910 on ClinicalTrials.gov