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Pediatric Influence of Cooling Duration on Efficacy in Cardiac Arrest Patients (P-ICECAP)

RECRUITINGN/ASponsored by University of Michigan
Actively Recruiting
PhaseN/A
SponsorUniversity of Michigan
Started2022-08-05
Est. completion2028-03-31
Eligibility
Age2 Days – 17 Years
Healthy vol.Accepted
Locations46 sites

Summary

This is a multicenter trial to establish the efficacy of cooling and the optimal duration of induced hypothermia for neuroprotection in pediatric comatose survivors of cardiac arrest. The study team hypothesizes that longer durations of cooling may improve either the proportion of children that attain a good neurobehavioral recovery or may result in better recovery among the proportion already categorized as having a good outcome.

Eligibility

Age: 2 Days – 17 YearsHealthy volunteers accepted
Inclusion criteria:

* Age 2 days to \< 18 years with corrected gestational age of at least 38 weeks
* Chest compressions for at least 2 minutes
* Coma or encephalopathy after resuscitation from Out-of-Hospital Cardiac Arrest (OHCA)
* Requires continuous mechanical ventilation through endotracheal tube or tracheostomy
* Definitive temperature control device initiated
* Randomization within 6 hours of Return of Spontaneous Circulation (ROSC)
* Informed consent from Legally Authorized Representative (LAR) including intent to maintain life support for 120 hours

Exclusion criteria:

* Glasgow Coma Motor Score (GCMS) = 6
* LAR does not speak English or Spanish
* Duration of Cardiopulmonary Resuscitation (CPR) \> 60 minutes
* Severe hemodynamic instability with continuous infusion of epinephrine or norepinephrine of 2 micrograms per kilogram per minute (μg/kg/minute) or initiation of Extracorporeal membrane oxygenation (ECMO)
* Pre-existing severe neurodevelopmental deficits with Pediatric Cerebral Performance Category (PCPC) =5 or progressive degenerative encephalopathy
* Pre-existing terminal illness, unlikely to survive to one year
* Cardiac arrest associated with brain, thoracic, or abdominal trauma
* Active and refractory severe bleeding prior to randomization
* Extensive burns or skin lesions incompatible with surface cooling
* Planned early withdrawal of life support before 120 hours
* Sickle cell anemia
* Pre-existing cryoglobulinemia
* Non-fatal drowning in ice covered water
* Central nervous system tumor with ongoing chemotherapy
* Previous enrollment in P-ICECAP trial
* Prisoner
* Chronic hypothermia
* New post-cardiac arrest diabetes insipidus
* Pregnancy

Conditions4

Cardiac Arrest, Out-Of-HospitalHeart DiseaseHypothermia, InducedHypoxia-Ischemia, Brain

Locations46 sites

University of Alabama at Birmingham / Children's of Alabama
Birmingham, Alabama, 35233
Michele Kong, MD205-638-9387mkong@uabmc.edu
Phoenix Children's Hospital
Phoenix, Arizona, 85016
F. Anthony Willyerd, MD602-471-5064fwillyerd@phoenixchildrens.com
Banner University Medical Center - Tucson
Tucson, Arizona, 85719
Mary Gaspers, MD
Memorial Health - Miller Children's and Women's Hospital of Long Beach
Long Beach, California, 90806-1701
Christopher Babbitt, MD562-933-8743CBabbitt@memorialcare.org
Children's Hospital of Los Angeles
Los Angeles, California, 90027
Bradley De Souza, MD323-361-8202bdesouza@chla.usc.edu

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