Registered outcomes11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

1 to 11 of 11

List	Outcome	Time frame	Description
Primary	Time to initial return of spontaneous circulation (ROSC)	At time of event	The primary outcome will be the time to initial ROSC. The investigator will compare time to initial ROSC between the standard of care and intervention periods.
Secondary	Return of spontaneous circulation	At time of event	Whether return of spontaneous circulation is achieved or not
Secondary	Time to sustained ROSC	At time of event	Time to sustained ROSC will be calculated from the time that paramedics arrive on scene to the time that sustained ROSC, defined as chest compressions not required for 20 minutes with persistent signs of circulation, is achieved.
Secondary	Survival	From time of event to ED admission	Survival to emergency department transfer to pediatric critical care unit (PCCU), if applicable: admitted to PCCU from external ED
Secondary	Survival - comparison between both arms	From time of event to hospital admission	Survival to hospital admission will be compared between standard of care and intervention periods
Secondary	PCCU/Hospital length of stay	From time of hospital/PCCU admission to discharge, up to 1 year	PCCU and hospital length of stay will be calculated from time of admission to the PCCU/hospital and time to discharge from PCCU/hospital, if applicable, between standard of care and intervention periods
Secondary	Survival to hospital discharge	Dependent on course of hospital stay, up to 1 year	Survival to hospital discharge will be compared between standard of care and intervention periods
Secondary	Post POHCA survival	Dependent on survival at 6 and 12 month period post POHCA event	Survival at 6 months and 12 months post-POHCA will be compared between standard of care and intervention periods
Secondary	Neurological status	From time of discharge and 6 and 12 months post POHCA event	The investigator will compare PCPC scores at discharge, 6- and 12-months post-POHCA between the standard of care and intervention periods
Secondary	Life Impact and Pediatric Quality of Life assessments	6 and 12 months post POHCA event	Life Impact assessment between 6 and 12 months: the investigator will use the Pediatric Quality of Life (PEDSQoL, Pediatrics Quality of Life) assessment tool at 6- and 12-months post-POHCA in all survivors and compare between standard of care and intervention periods. The score ranges from 0-100, with higher scores indicating better outcome.
Secondary	Life Impact and Pediatric Quality of Life assessments	6 and 12 months post POHCA event	Life Impact assessment between 6 and 12 months: the investigator will use the Daily Activities Scale at 6- and 12-months post-POHCA in all survivors and compare between standard of care and intervention periods. This scale is a subscore of the PEDSQoL tool with scores ranging from 0-100, with higher scores indicating better outcome.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
ClinicalTrials.govNo license stated
NIH RePORTER's clinical studies and project filesPublic domain

Each source's terms

ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
ClinicalTrials.govnone stated
NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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GET https://conductscience.org/api/trials/v1/NCT05166343/registered

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