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Pre-hospital ECMO in Advanced Resuscitation in Patients With Refractory Cardiac Arrest. ( SUB30 ) (SUB30)

Primary Purpose

Death, Sudden, Cardiac, Out-Of-Hospital Cardiac Arrest, Ventricular Fibrillation

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
ECMO resuscitation
Sponsored by
Barts & The London NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Death, Sudden, Cardiac focused on measuring Advanced life support (ALS), Extra-corporeal Membrane Oxygenation Resuscitation (ECMO)

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Adult patients who:

  • have a witnessed out-of-hospital cardiac arrest
  • a presumed cardiac aetiology to their cardiac arrest
  • receive bystander chest compressions within 3 minutes
  • remain in cardiac arrest at 20 minutes following the call to the emergency services or fail to sustain ROSC in the pre-hospital setting

Exclusion Criteria:

The following patients will not be suitable for entry into the study:

  • Known to be are visibly appear younger than 18 years old or older than 65 years.
  • Known or visible advanced pregnancy (when resuscitative hysterotomy should be performed)
  • No signs of life (physical movement or breathing) AND evidence of ineffective chest compressions suggested by:
  • absence of electrical activity at 20 minutes time out OR
  • end tidal carbon dioxide level of less than 1.3 kPa (10 mmHg)
  • Evidence from others present at the scene or patient examination that ECMO unlikely to benefit patient (e.g. advanced malignancy, severe frailty).

Sites / Locations

  • St Bartholomew's Hospital
  • London Ambulance Service Trust

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

ECMO resuscitation

Arm Description

6 patients who meet the eligibility criteria will be treated by pre-hospital advanced physician/ paramedic cardiac arrest team that is ECMO capable and can establish ECMO flow within 30 minutes of collapse

Outcomes

Primary Outcome Measures

Proportion of patients successfully established with pre-hospital ECPR
The primary endpoint is the proportion of patients successfully established with pre-hospital ECPR within 30 minutes of collapse

Secondary Outcome Measures

Ambulance dispatch
Number of patients not dispatched to as travel time too great/team unavailable
Successful cannulation
The number of patients successfully cannulated 31 and 45 minutes
Number of patients with return of spontaneous circulations (ROSC)
The number of patients patients who achieve ROSC prior to the 20 minutes timeout, number of patients in refractory cardiac arrest at 20 minutes in whom ROSC is achieved prior to ECMO flow
Emergency call-out time frame
The time interval between call to the emergency services and ECPR team arrival
Successful guide wire placement
The proportion of potentially supportable patients in whom guidewire placement is attempted and achieved
Incidence of ECPR-related complications
Assessment of ECPR-related complications, such as incidence of vascular damage, haemorrhage requiring transfusion and new organ dysfunction
Clinical outcome via FIM at 3 months
Assessment of functional status at hospital discharge using the Functional Independence Measure - FIM (18 item scale, measure of dependence. The higher the score, the more independent the patient is in performing the task).
Clinical outcome via MRS at 3 months
Assessment of functional status at hospital discharge using the modified Rankin Scale (MRS) (scale 0-6, measuring the degree of disability or dependence in the daily activities, where 0 is no symptoms and 6 is dead)
Duration of hospital stay
Assessment of health resources used for the duration of Intensive Care Unit stay
Number of acute hospital admissions post discharge
Assessment of health resources used for further hospital admissions following discharge.

Full Information

First Posted
October 2, 2018
Last Updated
November 16, 2020
Sponsor
Barts & The London NHS Trust
Collaborators
London's Air Ambulance, Bodychillz Ltd, Maquet Cardiopulmonary GmbH, Stryker Nordic
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1. Study Identification

Unique Protocol Identification Number
NCT03700125
Brief Title
Pre-hospital ECMO in Advanced Resuscitation in Patients With Refractory Cardiac Arrest. ( SUB30 )
Acronym
SUB30
Official Title
Feasibility Study of a Pre-hospital Extra-corporeal Membrane Oxygenation (ECMO) Capable Advanced Resuscitation Team at Achieving Blood Flow Within 30 Minutes in Patients With Refractory Cardiac Arrest.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
September 23, 2019 (Actual)
Primary Completion Date
May 31, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Barts & The London NHS Trust
Collaborators
London's Air Ambulance, Bodychillz Ltd, Maquet Cardiopulmonary GmbH, Stryker Nordic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To establish whether a pre-hospital advanced physician/ paramedic cardiac arrest team that is ECMO capable can establish ECMO flow within 30 minutes of collapse. The Sub30 study will investigate the technical and logistical feasibility of instituting pre-hospital Extracorporeal Cardiopulmonary Resuscitation (ECPR) within 30 minutes of collapse for selected patients (n=6) in a geographical sector of Greater London. It will achieve this through a unique collaboration between the primary emergency dispatch and response services (London Ambulance Service NHS Trust, LAS), pre-hospital practitioners (LAS and London Air Ambulance) and clinicians in ECMO (Barts Health NHS Trust).
Detailed Description
Every year, in London, the ambulance service treats over 4,000 patients who have a had a cardiac arrest (or their heart has stopped). Less than 1 in 10 patients survive to get home. Some of those who survive have severe brain damage since their brains did not receive blood and oxygen when their heart was stopped. The ambulance service in London manages to get to a patient, on average, 7 minutes following a 999 call. The paramedics are very skilled in restarting people's hearts and often manage this in less than 10 minutes. However, sometimes it can take much longer or not be possible. The risks of a patient dying or suffering brain damage increase the longer it takes to restart the heart, particularly after about 20-30 minutes. An extracorporeal membrane oxygenation (ECMO) machine may reduce these risks by pumping a patient's blood through an artificial lung and to their vital body organs - temporarily replacing the function of the heart and lungs. The ECMO is used in normal care to support patients after a cardiac arrest once a patient reaches the hospital, but in this study we want to see if the ECMO can be used very soon after the cardiac arrest is reported via the 999 call. In the Sub30 study, the ECMO team and machine to travel immediately to where the patient collapses rather than wait for the patient to be moved to a hospital. The study hypothesis is that the ECMO will be started faster and that this may improve patient survival and outcomes. The ECMO team consists of three senior doctors and a paramedic. They attend patients who have collapsed and start ECMO if standard advanced resuscitation techniques fail to restart the heart in 20 minutes. The team will aim to have the ECMO machine started within 30 minutes of the 999 call. The team have achieved this in training and the current study will assess whether it is possible to do this in six patients in real-life. A target of thirty minutes to achieve ECMO flow or return of spontaneous circulation (ROSC) is less than in published series to date. This can be achieved by: integration into an established pre-hospital emergency response services that aggressively pursue ROSC through optimised Advanced Life Support immediate deployment of an ECPR-capable cardiac arrest team as a primary resource, as opposed to delayed secondary deployment. Dispatch will be done by the established Advanced Paramedic Practitioner (APP) desk of London Ambulance Service, with the objective to reach the patient within 8-10 minutes of the 999 call. early placement of guide-wires into the femoral vessels during on-going conventional CPR, a procedure with low complication risk that does not commit the team to ECPR but will minimise the delay to ECPR support if conventional resuscitative techniques are not successful within 20 minutes facilitated guide-wire placement through real-time wireless ultrasound delivered to the operator through augmented reality smart glasses. Some out of hospital cardiac arrests (OHCA) are irreversible in nature and ECPR would not provide benefit to these patients. The ECPR team will not be task fixated on providing ECPR, but also supportive of the APP primary responders and provide ECPR only in settings of refractory cardiac arrest that fulfils the study criteria, that have been chosen based on best available evidence to identify those patients in whom ECPR is likely to be of benefit. If pre-hospital ECMO is feasible within 30 minutes of chest compressions starting, then a larger randomised controlled study of clinical and cost effectiveness is merited. Optimisation of the delivery of ECPR is vital, prior to a controlled study, in order to maximise any potential benefits for patients. Data from Sub30 will inform the design of such studies enabling an estimation of the size of any potential outcome benefits and the likely affordability for a healthcare service.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Death, Sudden, Cardiac, Out-Of-Hospital Cardiac Arrest, Ventricular Fibrillation, Cardiopulmonary Arrest With Successful Resuscitation
Keywords
Advanced life support (ALS), Extra-corporeal Membrane Oxygenation Resuscitation (ECMO)

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Single centre feasibility study of a complex intervention
Masking
None (Open Label)
Allocation
N/A
Enrollment
6 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ECMO resuscitation
Arm Type
Experimental
Arm Description
6 patients who meet the eligibility criteria will be treated by pre-hospital advanced physician/ paramedic cardiac arrest team that is ECMO capable and can establish ECMO flow within 30 minutes of collapse
Intervention Type
Procedure
Intervention Name(s)
ECMO resuscitation
Other Intervention Name(s)
Extracorporeal Membrane Oxygenation
Intervention Description
Extracorporeal Cardio-Pulmonary Resuscitation (ECPR) using ECMO within 30 minutes of cardiac arrest
Primary Outcome Measure Information:
Title
Proportion of patients successfully established with pre-hospital ECPR
Description
The primary endpoint is the proportion of patients successfully established with pre-hospital ECPR within 30 minutes of collapse
Time Frame
Within 30 minutes of collapse
Secondary Outcome Measure Information:
Title
Ambulance dispatch
Description
Number of patients not dispatched to as travel time too great/team unavailable
Time Frame
Within 30 minutes of collapse
Title
Successful cannulation
Description
The number of patients successfully cannulated 31 and 45 minutes
Time Frame
between 31 and 45 minutes; and 46 and 60 minutes.
Title
Number of patients with return of spontaneous circulations (ROSC)
Description
The number of patients patients who achieve ROSC prior to the 20 minutes timeout, number of patients in refractory cardiac arrest at 20 minutes in whom ROSC is achieved prior to ECMO flow
Time Frame
Within 20 minutes of cardiac arrest
Title
Emergency call-out time frame
Description
The time interval between call to the emergency services and ECPR team arrival
Time Frame
At 30 minutes after cardiac arrest
Title
Successful guide wire placement
Description
The proportion of potentially supportable patients in whom guidewire placement is attempted and achieved
Time Frame
Up to 30 minutes after cardiac arrest
Title
Incidence of ECPR-related complications
Description
Assessment of ECPR-related complications, such as incidence of vascular damage, haemorrhage requiring transfusion and new organ dysfunction
Time Frame
Duration of ECMO run, between 3 - 14 days
Title
Clinical outcome via FIM at 3 months
Description
Assessment of functional status at hospital discharge using the Functional Independence Measure - FIM (18 item scale, measure of dependence. The higher the score, the more independent the patient is in performing the task).
Time Frame
3 months
Title
Clinical outcome via MRS at 3 months
Description
Assessment of functional status at hospital discharge using the modified Rankin Scale (MRS) (scale 0-6, measuring the degree of disability or dependence in the daily activities, where 0 is no symptoms and 6 is dead)
Time Frame
3 months
Title
Duration of hospital stay
Description
Assessment of health resources used for the duration of Intensive Care Unit stay
Time Frame
1-3 months
Title
Number of acute hospital admissions post discharge
Description
Assessment of health resources used for further hospital admissions following discharge.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients who: have a witnessed out-of-hospital cardiac arrest a presumed cardiac aetiology to their cardiac arrest receive bystander chest compressions within 3 minutes remain in cardiac arrest at 20 minutes following the call to the emergency services or fail to sustain ROSC in the pre-hospital setting Exclusion Criteria: The following patients will not be suitable for entry into the study: Known to be are visibly appear younger than 18 years old or older than 65 years. Known or visible advanced pregnancy (when resuscitative hysterotomy should be performed) No signs of life (physical movement or breathing) AND evidence of ineffective chest compressions suggested by: absence of electrical activity at 20 minutes time out OR end tidal carbon dioxide level of less than 1.3 kPa (10 mmHg) Evidence from others present at the scene or patient examination that ECMO unlikely to benefit patient (e.g. advanced malignancy, severe frailty).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Simon Finney
Organizational Affiliation
Barts & The London NHS Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
St Bartholomew's Hospital
City
London
ZIP/Postal Code
EC1 6BQ
Country
United Kingdom
Facility Name
London Ambulance Service Trust
City
London
ZIP/Postal Code
SE1 0BW
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There is no plan to share study participant data
Citations:
PubMed Identifier
33403364
Citation
Singer B, Reynolds JC, Davies GE, Wrigley F, Whitbread M, Faulkner M, O'Brien B, Proudfoot AG, Mathur A, Evens T, Field J, Monk V, Finney SJ; International ECMO Network (ECMONet). Sub30: Protocol for the Sub30 feasibility study of a pre-hospital Extracorporeal membrane oxygenation (ECMO) capable advanced resuscitation team at achieving blood flow within 30 min in patients with refractory out-of-hospital cardiac arrest. Resusc Plus. 2020 Dec;4:100029. doi: 10.1016/j.resplu.2020.100029. Epub 2020 Oct 8.
Results Reference
derived
Links:
URL
https://www.qmul.ac.uk/whri/clinical-activities/cvctu/trials-portfolio/sub-30/
Description
Bart Cardiovascular Clinical Trials Unit (CVCTU) portfolio - SUB30 study

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Pre-hospital ECMO in Advanced Resuscitation in Patients With Refractory Cardiac Arrest. ( SUB30 )

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