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Recruiting NCT05166343

POHCA Resuscitation: Evaluation of IM Epinephrine

Phase II / Phase III Interventional Pediatric Out-of-Hospital Cardiac Arrest

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Epinephrine Injection.
Who it may be relevant to
Registry conditions: Pediatric Out-of-Hospital Cardiac Arrest. Basic parameters: 1 Day — 17 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Canada
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Pediatric Out-of-Hospital Cardiac Arrest Resuscitation: Evaluation of IM Epinephrine (The PRIME Trial)

Overview

This is a pragmatic, two-arm, open-label, prospective stepped-wedge cluster quasi randomized control trial (SW-CRCT) looking to evaluate early intramuscular (IM) epinephrine in the management of pediatric out-of-hospital cardiac arrest (POHCA).

Detailed description

IM epinephrine may provide a more efficient means of administering the initial epinephrine dose (versus IV/IO administration) to a child experiencing pediatric out of hospital cardiac arrest (POHCA) with no greater risk of harm. In so doing, this may improve the short- and long-term outcomes of these patients. There is an abundance of literature detailing the risk/benefit profile of IM epinephrine use in anaphylaxis; however, there is no human data on this topic as it relates to cardiac arrest. Important knowledge gaps include whether the use of IM epinephrine via autoinjector and/or pre-filled syringe leads to faster administration of the initial doses of epinephrine without delaying time to definitive epinephrine (via IV/IO) and the impact on time to initial and sustained return of spontaneous circulation (ROSC). This trial will be the first to examine the role of IM epinephrine via autoinjector/pre-filled syringe in POHCA.

Interventions

  • Drug Epinephrine Injection
    Epinephrine administered via sterile epinephrine injection USP, by 0.3mg or 0.5mg epinephrine auto-injector(s) and/or pre-filled syringe (exact dose).

Primary outcome measures

  • Time to initial return of spontaneous circulation (ROSC) [Time frame: At time of event]
Secondary outcome measures (10)
  • Return of spontaneous circulation [Time frame: At time of event]
  • Time to sustained ROSC [Time frame: At time of event]
  • Survival [Time frame: From time of event to ED admission]
  • Survival - comparison between both arms [Time frame: From time of event to hospital admission]
  • PCCU/Hospital length of stay [Time frame: From time of hospital/PCCU admission to discharge, up to 1 year]
  • Survival to hospital discharge [Time frame: Dependent on course of hospital stay, up to 1 year]
  • Post POHCA survival [Time frame: Dependent on survival at 6 and 12 month period post POHCA event]
  • Neurological status [Time frame: From time of discharge and 6 and 12 months post POHCA event]
  • Life Impact and Pediatric Quality of Life assessments [Time frame: 6 and 12 months post POHCA event]
  • Life Impact and Pediatric Quality of Life assessments [Time frame: 6 and 12 months post POHCA event]

Eligibility criteria

Inclusion criteria

  • Children aged 1 day to and including 17 years experiencing an out-of-hospital cardiac arrest (OHCA)
  • Must be receiving at least 1 minute of CPR by trained first responders (police, fire, or paramedic services)

Exclusion criteria

\- Children who experience OHCA due to an obvious traumatic event.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Supportive care

Study locations

Canada · 1 center
  • Children's Hospital - London Health Sciences Centre — London

Publications

  • Idrees S, Assaf M, Davis M, Garcia-Bournissen F, Loosley J, Miller MR, Tijssen JA. Evaluating intramuscular epinephrine in pediatric out-of-hospital cardiac arrest (the PRIME trial): study protocol for a multi-centre, stepped-wedge cluster quasi-randomized controlled trial. Trials. 2026 Jun 8. doi: 10.1186/s13063-026-09776-3. Online ahead of print. PMID 42260675

Identifiers

NCT: NCT05166343 · PRIME-1

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗