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Emergency Preservation and Resuscitation (EPR) for Cardiac Arrest From Trauma (EPR-CAT)

Primary Purpose

Cardiac Arrest From Trauma

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Emergency preservation and resuscitation
Standard resuscitation
Sponsored by
University of Maryland, Baltimore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiac Arrest From Trauma focused on measuring trauma, cardiac arrest, hemorrhagic shock

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Penetrating trauma with clinical suspicion of exsanguinating hemorrhage
  • At least 1 sign of life at the scene (pulse, respiratory efforts, spontaneous movements, reactive pupils)
  • Loss of pulse <5 min prior to Emergency Department (ED) arrival or in ED or operating room
  • ED thoracotomy performed without immediate return of a palpable pulse in the carotid arteries after clamping the descending thoracic aorta

Exclusion Criteria:

  • No signs of life for >5 min prior to the decision to initiate EPR
  • Obvious non-survivable injury
  • Suggestion of traumatic brain injury, such as significant facial or cranial distortion
  • Electrical asystole
  • Rapid external assessment of the injuries suggests massive tissue trauma or blunt trauma involving multiple body regions
  • Pregnancy
  • Prisoners

Sites / Locations

  • University of MarylandRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Concurrent controls

Emergency preservation and resuscitation

Arm Description

These subjects would undergo standard resuscitative efforts.

These subjects would undergo the complete EPR protocol, including rapid induction of hypothermia, resuscitative surgery, and resuscitation with cardiopulmonary bypass.

Outcomes

Primary Outcome Measures

The primary endpoint is survival to hospital discharge without major disability (Glasgow Outcome Scale-Extended >5).

Secondary Outcome Measures

Feasibility of initiating EPR (cooling and achieving goal brain temperature)
Survival
Neurologic functional outcome
Multiple organ system dysfunction

Full Information

First Posted
January 4, 2010
Last Updated
June 11, 2023
Sponsor
University of Maryland, Baltimore
Collaborators
Cook County Health
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1. Study Identification

Unique Protocol Identification Number
NCT01042015
Brief Title
Emergency Preservation and Resuscitation (EPR) for Cardiac Arrest From Trauma
Acronym
EPR-CAT
Official Title
Emergency Preservation and Resuscitation for Cardiac Arrest From Trauma
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 2016 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Maryland, Baltimore
Collaborators
Cook County Health

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The goal of this study is to rapidly cool trauma victims who have suffered cardiac arrest from bleeding with a flush of ice-cold sodium chloride to preserve the patient to enable surgical control of bleeding, followed by delayed resuscitation with cardiopulmonary bypass.
Detailed Description
The intent of the technique to be studied is to induce a state of hypothermic preservation in trauma victims who have exsanguinated to the point of cardiac arrest. In appropriately selected subjects, after an initial emergency attempt at resuscitation with standard techniques, an arterial catheter will be inserted into the descending thoracic aorta. Using appropriate tubing, pump, and heat exchanger,a large quantity of ice-cold saline (0.9% Sodium Chloride for Injection USP) will be pumped as rapidly as possible into the aorta with the goal of cooling the brain (tympanic membrane temperature, Tty) to <10 C. If possible, a large venous catheter will be placed and recirculation of fluid established. Once the subject has been sufficiently cooled, bleeding will be controlled surgically. The subject will then be resuscitated and rewarmed with full cardiopulmonary bypass. The goal is to improve neurologically-intact survival in these patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Arrest From Trauma
Keywords
trauma, cardiac arrest, hemorrhagic shock

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Concurrent controls
Arm Type
Active Comparator
Arm Description
These subjects would undergo standard resuscitative efforts.
Arm Title
Emergency preservation and resuscitation
Arm Type
Experimental
Arm Description
These subjects would undergo the complete EPR protocol, including rapid induction of hypothermia, resuscitative surgery, and resuscitation with cardiopulmonary bypass.
Intervention Type
Combination Product
Intervention Name(s)
Emergency preservation and resuscitation
Intervention Description
This involves the induction of profound hypothermia using a flush of ice-cold saline into the aorta. Once hypothermia is achieved, the subject would undergo rapid operative interventions to control bleeding followed by resuscitation/rewarming with cardiopulmonary bypass.
Intervention Type
Other
Intervention Name(s)
Standard resuscitation
Intervention Description
Standard resuscitation includes an emergency department thoracotomy, open cardiac massage, and fluid resuscitation.
Primary Outcome Measure Information:
Title
The primary endpoint is survival to hospital discharge without major disability (Glasgow Outcome Scale-Extended >5).
Time Frame
Hospital discharge
Secondary Outcome Measure Information:
Title
Feasibility of initiating EPR (cooling and achieving goal brain temperature)
Time Frame
1 hour
Title
Survival
Time Frame
28 days
Title
Neurologic functional outcome
Time Frame
12 months
Title
Multiple organ system dysfunction
Time Frame
During the initial hospitalization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Penetrating trauma with clinical suspicion of exsanguinating hemorrhage At least 1 sign of life at the scene (pulse, respiratory efforts, spontaneous movements, reactive pupils) Loss of pulse <5 min prior to Emergency Department (ED) arrival or in ED or operating room ED thoracotomy performed without immediate return of a palpable pulse in the carotid arteries after clamping the descending thoracic aorta Exclusion Criteria: No signs of life for >5 min prior to the decision to initiate EPR Obvious non-survivable injury Suggestion of traumatic brain injury, such as significant facial or cranial distortion Electrical asystole Rapid external assessment of the injuries suggests massive tissue trauma or blunt trauma involving multiple body regions Pregnancy Prisoners
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Samuel A Tisherman, MD
Phone
410-328-9781
Email
stisherman@som.umaryland.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Leslie Sult
Phone
410-299-3738
Email
lsult@som.umaryland.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Samuel A Tisherman, MD
Organizational Affiliation
University of Maryland, Baltimore
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Maryland
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Samuel A Tisherman, MD
Phone
410-328-9781
Email
stisherman@som.umaryland.edu
First Name & Middle Initial & Last Name & Degree
Leslie Sult, RN
Phone
410-328-0288
Email
lsult@som.umaryland.edu
First Name & Middle Initial & Last Name & Degree
Thomas Scalea, MD
First Name & Middle Initial & Last Name & Degree
James O'Connor, MD
First Name & Middle Initial & Last Name & Degree
Joseph Rabin, MD
First Name & Middle Initial & Last Name & Degree
Samuel A Tisherman, MD
First Name & Middle Initial & Last Name & Degree
Kristopher Deatrick, MD
First Name & Middle Initial & Last Name & Degree
David Efron, MD
First Name & Middle Initial & Last Name & Degree
Rishi Kundi, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
28538639
Citation
Tisherman SA, Alam HB, Rhee PM, Scalea TM, Drabek T, Forsythe RM, Kochanek PM. Development of the emergency preservation and resuscitation for cardiac arrest from trauma clinical trial. J Trauma Acute Care Surg. 2017 Nov;83(5):803-809. doi: 10.1097/TA.0000000000001585.
Results Reference
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Emergency Preservation and Resuscitation (EPR) for Cardiac Arrest From Trauma

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