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Initiation of Cooling by EMS to Promote Adoption of In-hospital Hypothermia in Cardiac Arrest Survivors

Primary Purpose

Out of Hospital Cardiac Arrest

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Pre-hospital cooling
Sponsored by
Sunnybrook Health Sciences Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Out of Hospital Cardiac Arrest focused on measuring Therapeutic Hypothermia, Cardiac arrest

Eligibility Criteria

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

Inclusion Criteria:

  • Pulseless OHCA in the study communities (any rhythm, initial rhythm will be recorded)
  • Age equal to or greater than 18 years
  • Defibrillation and/or chest compressions by EMS providers (including fire fighters)
  • Return of spontaneous circulation (ROSC) sustained for greater than or equal to 5 minutes
  • Patient is unresponsive to verbal stimulus using AVPU (Alert, Voice, Pain, Unresponsive) scale
  • Patient is endotracheally intubated
  • SBP equal to or greater than 100 mm Hg (even if needing dopamine)

Exclusion Criteria:

  • Trauma (including burns) associated with cardiac arrest
  • Sepsis or serious infection suspected as cause of cardiac arrest
  • Clinical evidence of active severe bleeding
  • Suspected hypothermic cardiac arrest
  • Known coagulopathy (medical history or medications; ASA and clopidogrel are permitted)
  • Any verbal or written do-not-resuscitate (DNR)
  • Obviously pregnant
  • Known Prisoner

Sites / Locations

  • Peel Emergency Medical Services
  • Halton Emergency Medical Services
  • Toronto Emergency Medical Services

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Pre-hospital cooling

Usual pre-hospital care

Arm Description

Patients in this arm will receive pre-hospital cooling by paramedics. This treatment includes placement of surface ice-pacs, initiation of an intravenous infusion of cold saline, and wrist and ankle bands with text to remind in-hospital clinicians to continue therapeutic hypothermia.

Patients in this arm will receive usual post-resuscitation care by paramedics. Usual post-resuscitation care does not include initiation of cooling in the pre-hospital setting.

Outcomes

Primary Outcome Measures

Success of in-hospital cooling
The primary outcome is the proportion of included patients that are successfully cooled to reach target temperature of 32 to 34 degrees Celsius within 6 hours of emergency department arrival.

Secondary Outcome Measures

Mortality at hospital discharge
Proportion of deaths at hospital discharge
Mortality during transport
Proportion of patients that die after randomization and during transport to hospital.
Mortality during 6 hours
Proportion of patients that die within 6 hours of emergency department arrival
Cooling ever in hospital
Proportion of patients for whom in-hospital therapeutic hypothermia is initiated or continued within 24 hours of emergency department arrival
Median Modified Rankin score at hospital discharge
The median modified Rankin score at hospital discharge
Good neurological outcome
The proportion of patients with Modified Rankin Scale = 0, 1, or 2 at hospital discharge.
Time of transport to hospital
Mean time (minutes) from arrival of paramedics on the scene to arrival and transport of patient to emergency department.

Full Information

First Posted
October 31, 2011
Last Updated
December 16, 2016
Sponsor
Sunnybrook Health Sciences Centre
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1. Study Identification

Unique Protocol Identification Number
NCT01528475
Brief Title
Initiation of Cooling by EMS to Promote Adoption of In-hospital Hypothermia in Cardiac Arrest Survivors
Official Title
Initiation of Cooling by Emergency Medical Services to Promote the Adoption of In-hospital Therapeutic Hypothermia in Cardiac Arrest Survivors: the ICE-PACS Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Completed
Study Start Date
July 2012 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
June 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sunnybrook Health Sciences Centre

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a large pragmatic, randomized controlled trial comparing pre-hospital initiation of therapeutic hypothermia by Emergency Medical Services (EMS) providers to conventional post-resuscitation care. The goal of this trial is to increase the proportion of cardiac arrest patients that are appropriately treated in-hospital with therapeutic hypothermia to reach the target body temperature within 6 hours of hospital arrival. The investigators believe that EMS-initiation of cooling will be a powerful reminder to in-hospital clinicians to continue therapeutic hypothermia, and will lead to care improvements across a health system.
Detailed Description
This is a large pragmatic, randomized controlled trial comparing pre-hospital initiation of therapeutic hypothermia by Emergency Medical Services (EMS) providers to conventional post-resuscitation care. The goal of this trial is to increase the proportion of cardiac arrest patients that are appropriately treated in-hospital with therapeutic hypothermia to reach the target body temperature within 6 hours of hospital arrival. The investigators believe that EMS-initiation of cooling will be a powerful reminder to in-hospital clinicians to continue therapeutic hypothermia, and will lead to care improvements across a health system. This study builds on our previous work using large hospital networks hospitals to improve the delivery of evidence-based practice. The primary research question is as follows: Does pre-hospital initiation of therapeutic hypothermia by EMS providers increase the proportion of comatose out of hospital cardiac arrest patients with return of spontaneous circulation (ROSC) that are successfully cooled to a target temperature of 32 to 34 degrees Celsius within 6 hours of emergency department arrival, compared to usual post-resuscitation care provided in the field? The primary outcome is the proportion of included patients that are successfully cooled to reach target temperature of 32 to 34 degrees Celsius within 6 hours of emergency department arrival.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Out of Hospital Cardiac Arrest
Keywords
Therapeutic Hypothermia, Cardiac arrest

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
585 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pre-hospital cooling
Arm Type
Active Comparator
Arm Description
Patients in this arm will receive pre-hospital cooling by paramedics. This treatment includes placement of surface ice-pacs, initiation of an intravenous infusion of cold saline, and wrist and ankle bands with text to remind in-hospital clinicians to continue therapeutic hypothermia.
Arm Title
Usual pre-hospital care
Arm Type
No Intervention
Arm Description
Patients in this arm will receive usual post-resuscitation care by paramedics. Usual post-resuscitation care does not include initiation of cooling in the pre-hospital setting.
Intervention Type
Behavioral
Intervention Name(s)
Pre-hospital cooling
Intervention Description
Patients in this arm will receive pre-hospital cooling by paramedics. This treatment includes placement of surface ice-pacs on the neck, groin, and axillae; midazolam to prevent shivering; initiation of an intravenous infusion of cold saline; and wrist and ankle bands with text to remind in-hospital clinicians to continue therapeutic hypothermia.
Primary Outcome Measure Information:
Title
Success of in-hospital cooling
Description
The primary outcome is the proportion of included patients that are successfully cooled to reach target temperature of 32 to 34 degrees Celsius within 6 hours of emergency department arrival.
Time Frame
within 6 hours of emergency department arrival
Secondary Outcome Measure Information:
Title
Mortality at hospital discharge
Description
Proportion of deaths at hospital discharge
Time Frame
Hospital discharge
Title
Mortality during transport
Description
Proportion of patients that die after randomization and during transport to hospital.
Time Frame
During transport to hospital
Title
Mortality during 6 hours
Description
Proportion of patients that die within 6 hours of emergency department arrival
Time Frame
Within 6 hours of emergency department arrival
Title
Cooling ever in hospital
Description
Proportion of patients for whom in-hospital therapeutic hypothermia is initiated or continued within 24 hours of emergency department arrival
Time Frame
within 24 hours of emergency department arrival
Title
Median Modified Rankin score at hospital discharge
Description
The median modified Rankin score at hospital discharge
Time Frame
hospital discharge
Title
Good neurological outcome
Description
The proportion of patients with Modified Rankin Scale = 0, 1, or 2 at hospital discharge.
Time Frame
hospital discharge
Title
Time of transport to hospital
Description
Mean time (minutes) from arrival of paramedics on the scene to arrival and transport of patient to emergency department.
Time Frame
During transport to hospital

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pulseless OHCA in the study communities (any rhythm, initial rhythm will be recorded) Age equal to or greater than 18 years Defibrillation and/or chest compressions by EMS providers (including fire fighters) Return of spontaneous circulation (ROSC) sustained for greater than or equal to 5 minutes Patient is unresponsive to verbal stimulus using AVPU (Alert, Voice, Pain, Unresponsive) scale Patient is endotracheally intubated SBP equal to or greater than 100 mm Hg (even if needing dopamine) Exclusion Criteria: Trauma (including burns) associated with cardiac arrest Sepsis or serious infection suspected as cause of cardiac arrest Clinical evidence of active severe bleeding Suspected hypothermic cardiac arrest Known coagulopathy (medical history or medications; ASA and clopidogrel are permitted) Any verbal or written do-not-resuscitate (DNR) Obviously pregnant Known Prisoner
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Damon Scales, MD
Organizational Affiliation
Sunnybrook Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Laurie Morrison, M.D.
Organizational Affiliation
Unity Health Toronto
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Steven Brooks, M.D.
Organizational Affiliation
Clinical Scientist
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Rick Verbeek, MD
Organizational Affiliation
Sunnybrook Centre for Prehospital Medicine
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Sheldon Cheskes, MD
Organizational Affiliation
Sunnybrook Centre for Prehospital Medicine
Official's Role
Study Chair
Facility Information:
Facility Name
Peel Emergency Medical Services
City
Mississauga
State/Province
Ontario
Country
Canada
Facility Name
Halton Emergency Medical Services
City
Oakville
State/Province
Ontario
Country
Canada
Facility Name
Toronto Emergency Medical Services
City
Toronto
State/Province
Ontario
Country
Canada

12. IPD Sharing Statement

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Initiation of Cooling by EMS to Promote Adoption of In-hospital Hypothermia in Cardiac Arrest Survivors

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