MedPath

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

Phase 2
Recruiting
Conditions
Cardiac Arrest From Trauma
Registration Number
NCT01042015
Lead Sponsor
University of Maryland, Baltimore
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.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
20
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
The primary endpoint is survival to hospital discharge without major disability (Glasgow Outcome Scale-Extended >5).Hospital discharge
Secondary Outcome Measures
NameTimeMethod
Feasibility of initiating EPR (cooling and achieving goal brain temperature)1 hour
Multiple organ system dysfunctionDuring the initial hospitalization
Neurologic functional outcome12 months
Survival28 days

Trial Locations

Locations (1)

University of Maryland

🇺🇸

Baltimore, Maryland, United States

University of Maryland
🇺🇸Baltimore, Maryland, United States
Samuel A Tisherman, MD
Principal Investigator
Leslie Sult, RN
Contact
410-328-0288
lsult@som.umaryland.edu
Thomas Scalea, MD
Sub Investigator
James O'Connor, MD
Sub Investigator
Joseph Rabin, MD
Sub Investigator
Kristopher Deatrick, MD
Sub Investigator
David Efron, MD
Sub Investigator
Rishi Kundi, MD
Sub Investigator
Deborah Stein, MD
Sub Investigator
Yvonne Chung, MD
Sub Investigator
Douglas Anderson, DO
Sub Investigator

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