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Quality of Pediatric Resuscitation in a Multicenter Collaborative

Quality of Pediatric Resuscitation in a Multicenter Collaborative: An Observational Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02708134
Acronym
pediRES-Q
Enrollment
7000
Registered
2016-03-15
Start date
2016-05-02
Completion date
2030-01-31
Last updated
2025-10-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrest, Cardiopulmonary Arrest

Keywords

Chest compressions, Cardiopulmonary Resuscitation, Pediatric

Brief summary

This is a prospective, observational, multi-center cohort study of pediatric cardiac arrests. The purpose of the study is to determine the association between chest compression mechanics (rate, depth, flow fraction, compression release) and patient outcomes. In addition, the investigators will determine the association of post cardiac arrest care with patient outcomes.

Detailed description

Cardiac arrests in children are a major public health problem. Thousands of children each year in the USA are treated with cardiopulmonary resuscitation (CPR) and managed after their cardiac arrest. Neurological outcomes following these in-hospital CPR events are often abnormal. As children with neurological deficits following CPR are a major burden for families and society, improving neurological outcomes through superior chest compression delivery during CPR and optimal care and management after cardiac arrest is an important clinical goal. Therefore, the objective of this investigation is to obtain evidentiary support to associate the relationship of quantitative CPR quality data (depth, rate, chest compressions (CC) fraction, compression release) during CPR, post-cardiac arrest care (PCAC) and patient survival in those children who suffer an arrest within the study (RES-Q) Network.

Interventions

None listed

Sponsors

Zoll Medical Corporation
CollaboratorINDUSTRY
Children's Hospital of Philadelphia
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Patient received chest compressions for at least 1 minute * Patient between gestational age ≥37 weeks and 18 years of age

Exclusion criteria

* Patient on veno-arterial extracorporeal membrane oxygenation (ECMO) therapy at beginning of CPR event

Design outcomes

Primary

MeasureTime frameDescription
Aggregate score composed of American Heart Association (AHA) recommended depth, rate, and chest compression fraction during CPR10 YearsPrimary outcome: Guideline-compliant CPR which will be determined by an aggregate score comprised of the following three components: depth, rate, and chest compression fraction. The three components will be analyzed in 30 and 60 second epochs. Guideline-compliant CPR requires that each component meet the following criteria: 1) Age-determined American Heart Association (AHA) guideline recommended depth; 2) rate ≥ 90 and ≤ 120 CC/min; and 3) CC Fraction ≥ 0.80. Depth, rate, and CC Fraction will be calculated for each epoch and an aggregate score will be assigned. The primary analysis will be performed on that total score.

Countries

Australia, Brazil, Canada, Colombia, Italy, Japan, Netherlands, New Zealand, Singapore, South Korea, Spain, Taiwan, Thailand, United Kingdom, United States

Contacts

Primary ContactVinay Nadkarni, MD, MS
nadkarni@chop.edu215-590-7430
Backup ContactKathryn Graham
grahamk1@chop.edu215-590-1859

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026