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RecruitingNCT07890610PEDICAUpdated Oct 22, 2026

Physiology-directed Epinephrine Dosing in Pediatric Cardiac Arrest

An observational study in Cardiac Arrest (CA), sponsored by Children's Hospital of Philadelphia. Recruiting at 22 sites in United States. Open to participants aged 37 Weeks to 18 Years. Per ClinicalTrials.gov, last updated 2026-10-22.

Sponsored by Children's Hospital of Philadelphia · Observational

From the registry’s dates

  • Started Jul 2024; still recruiting 2 years 3 months later.
Updated Oct 22, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,620
Ages
37 Weeks to 18 Years
Sex
All
01

Study summary

This is a prospective, observational, multi-center cohort study of pediatric cardiac arrests. The purpose of this study is to evaluate the physiologic response to epinephrine as an outcome discriminator in pediatric in-hospital cardiac arrest (IHCA). In addition, the investigators will determine optimal epinephrine dosing strategies based on the initial physiologic response to epinephrine, and to develop machine learning (ML) algorithms to guide intra-arrest therapy.

02

Conditions studied

  • Cardiac Arrest (CA)

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Keywords

  • Pediatric
  • Epinephrine
03

In context

Heart Arrest

984 studies on the registry are indexed under Heart Arrest; 227 are open to participants now.

This study's planned enrollment of 1,620 is above the median of 196 across 394 observational studies indexed under Heart Arrest.

Browse Heart Arrest studies →

Lead sponsor

Children's Hospital of Philadelphia is the lead sponsor of 488 studies on the registry; 91 are open to participants now.

Of its 28 completed or terminated interventional studies of FDA-regulated products, 22 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
37 Weeks to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Data will be collected from pediatric cardiac arrest events as part of standard clinical operations.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Arrest in an ICU
  • Patients received chest compressions for at least 1 minute

Exclusion criteria

Exclusion Criteria:

  • Lack of commitment to aggressive therapies (e.g., CPR performed as part of end-of-life care)
  • Brain death determination prior to CPR
  • Out-of-hospital cardiac arrest was the reason for initial admission to the hospital (known poor outcomes)
  • Supported by Veno-Arterial Extra Corporeal Membrane Oxygenation at the start of CPR
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,620 participants (estimated)
Patient registry
No

Groups and cohorts

  • Pediatric Cardiac Arrests

    Pediatric cardiac arrests requiring chest compressions for at least 1 minute occurring in an ICU identified as part of standard clinical operations.

06

What researchers measure

Primary outcomes

  1. Return of Spontaneous Circulation (ROSC) lasting 20 minutes

    Sustained return of ROSC ≥20 minutes

    Time frame: Duration of CPR event through 20 minutes after CPR

Secondary outcomes

  1. Survival with a favorable neurologic outcome

    Survival to hospital discharge with a favorable neurologic outcome (Pediatric Cerebral Performance Category (PCPC) score (scored on a scale of 1-6) at hospital discharge of 1 (normal), 2 (mild disability) or no worse than baseline).

    Time frame: From baseline (assessed prior to admission, or new in-hospital baseline assessed no more than 30 days prior to cardiac arrest for patients hospitalized >90 days) to the assessment at hospital discharge, estimated average of 6-12 months

  2. Survival with no new morbidity (change in Functional Status Score (FSS) from baseline of < 3 points)

    FSS is scored on a scale of 1-5 (lower number is better function) across 6 functional categories (mental status, sensory, communication, motor function, feeding, respiratory).

    Time frame: From baseline (assessed prior to admission, or new in-hospital baseline assessed no more than 30 days prior to cardiac arrest for patients hospitalized >90 days) to the assessment at hospital discharge, estimated average of 6-12 months

07

Study locations

22 of 22 sites recruiting
  • CHOC
    Orange, California 92868, United States
    Recruiting
  • Stanford Medicine Children's Health
    Stanford, California 94305, United States
    Recruiting
  • Children's Hospital Colorado
    Denver, Colorado 80045, United States
    Recruiting
  • Nemours Children's Health
    Wilmington, Delaware 19803, United States
    Recruiting
  • Children's Healthcare of Atlanta
    Atlanta, Georgia 30303, United States
    Recruiting
  • Comer Children's Hospital
    Chicago, Illinois 60637, United States
    Recruiting
  • Riley Children's Health
    Indianapolis, Indiana 46202, United States
    Recruiting
  • Stead Family Children's Hospital
    Iowa City, Iowa 52242, United States
    Recruiting
  • Boston Children's Hospital
    Boston, Massachusetts 02115, United States
    Recruiting
  • Washington University in St. Louis
    St Louis, Missouri 63110, United States
    Recruiting
  • Cohen Children's Medical Center
    New Hyde Park, New York 11040, United States
    Recruiting
  • Columbia University Irving Medical Center
    New York, New York 10032, United States
    Recruiting
  • UNC Children's Hospital
    Chapel Hill, North Carolina 27599, United States
    Recruiting
  • Cincinnati Children's Hospital Medical Center
    Cincinnati, Ohio 45229, United States
    Recruiting
  • Nationwide Children's Hospital
    Columbus, Ohio 43205, United States
    Recruiting
  • Children's Hospital of Philadelphia
    Philadelphia, Pennsylvania 19104, United States
    Recruiting
  • Dell Children's Medical Center
    Austin, Texas 78723, United States
    Recruiting
  • Medical City Children's Hospital
    Dallas, Texas 75230, United States
    Recruiting
  • University of Texas Southwestern Medical Center
    Dallas, Texas 75390, United States
    Recruiting
  • Children's Hospital of Richmond at VCU
    Richmond, Virginia 23219, United States
    Recruiting
  • Seattle Children's
    Seattle, Washington 98105, United States
    Recruiting
  • Children's Wisconsin
    Milwaukee, Wisconsin 53226, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — At the conclusion of the study, we will create a public use data set containing all analytical variables. The public use data set will contain a randomly generated subject ID but will not contain any personal or site identifiers. The cleaned, item-level spreadsheet data for all variables will be shared openly, along with example quantifications and transformations from initial raw data. Final files used to generate specific analyses to answer the Specific Aims and related results will also be shared.

Supporting information: Study protocol, Statistical analysis plan

Time frame: The public use data set will be made available within three months of completion of the primary manuscript. If the primary manuscript isn't published within 12 months of the end of funding, we will proceed with publishing the public use data set. The duration of preservation and sharing of the data will be a minimum of 10 years after the funding period.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 22, 2026
Show all 1 update
  1. Oct 22, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07890610
Responsible party
Sponsor
First posted
Oct 22, 2026
Start date
Jul 1, 2024
Primary completion
Jun 30, 2029 (estimated)
Completion
Jun 30, 2029 (estimated)
Last update
Oct 22, 2026

Study contacts

Jessica Goldstein
Contact
goldsteij1@chop.edu
215-590-1859
CHOP RSC Clinical Research Program Manager
Contact
grahamk1@chop.edu
215-590-1859
Ryan Morgan, MD, MTR
principal investigator · Children's Hospital of Philadelphia

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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