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Bedside Cranial Ultrasound for Risk-Stratified Imaging in Pediatric Acute Brain Injury

Bedside Cranial Point-of-Care Ultrasound (cPOCUS) for Risk-Stratified Imaging in Pediatric Acute Brain Injury: A Prospective Diagnostic-Accuracy and Longitudinal Biomarker Cohort Study (CUPID-Peds)

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07772323
Acronym
CUPID-Peds
Enrollment
220
Registered
2026-08-19
Start date
2026-11-30
Completion date
2028-11-30
Last updated
2026-08-19

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

Conditions

Acute Brain Injury, Brain Neoplasm, Hydrocephalus, Hypoxia-Ischemia, Brain, Intracranial Hemorrhage, Stroke, Traumatic Brain Injury

Keywords

cranial ultrasound, point-of-care ultrasound, cPOCUS, transcranial B-mode ultrasound, pediatric neuroimaging, head CT, midline shift, diagnostic accuracy, radiation reduction, neurocritical care

Brief summary

Acute brain injury (ABI) is a leading cause of death and long-term disability in children. Diagnosis depends on fast neuroimaging, and head computed tomography (CT) is the bedside reference standard despite exposing the developing brain to ionizing radiation. A safe, portable, radiation-free bedside tool is needed to help decide which children need a head CT, to speed CT when injury is present, and to safely monitor injured children between scans. This study evaluates B-mode cranial point-of-care ultrasound (cPOCUS) performed through the temporal (and frontal) bone windows in children undergoing a clinically indicated head CT in the pediatric emergency department (ED) and pediatric intensive care unit (PICU). Children's thin skulls provide adequate acoustic windows in more than 95% of cases. cPOCUS is acquired by trained research scanners within 6 hours of head CT and interpreted offline by two blinded expert readers; the radiology CT report is the diagnostic gold standard. This is a prospective observational study; cPOCUS results are not returned to the clinical team in real time and do not change clinical care.

Detailed description

Prospective observational cohort study of children undergoing clinically indicated head CT for suspected acute brain injury (ABI) in the pediatric ED and PICU at the Children's Hospital of Richmond at Virginia Commonwealth University (CHoR-VCU). Within 6 hours of the head CT, trained research scanners (acquisition-only role) acquire standardized B-mode cranial point-of-care ultrasound (cPOCUS) using 1-3 MHz phased-array probes through bilateral temporal and frontal windows, exporting de-identified 3-5 second cine loops at and around the midbrain plane to an encrypted offline reading workstation. Two pre-specified expert readers interpret the studies independently and offline in Horos, each blinded to the clinical course, the head-CT report, and one another; discordant cases are resolved by joint re-read to a single adjudicated consensus interpretation, which serves as the cPOCUS index test. The attending radiology head-CT report is the diagnostic gold (reference) standard. Because reads are not returned to the clinical team in real time, cPOCUS is not an assigned intervention, and the endpoints are diagnostic test characteristics, there is no change to clinical care.

Interventions

None listed

Sponsors

Virginia Commonwealth University
Lead SponsorOTHER
UMass Chan Medical School
CollaboratorUNKNOWN
Atrium Health Levine Children's Hospital
CollaboratorUNKNOWN
Children's Hospital of Richmond at VCU
CollaboratorUNKNOWN

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
2 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Children 2 to 17 years of age * Undergoing a clinically indicated (standard-of-care) head CT for suspected acute brain injury (including trauma, headache with neurologic findings, altered mental status, focal deficit, seizure, post-cardiac-arrest, oncologic neurologic emergency, or intracranial infection) * Seen in the pediatric Emergency Department or Pediatric Intensive Care Unit at the Children's Hospital of Richmond at VCU (CHoR-VCU) * Consent obtainable from a legally authorized representative (LAR) * Cranial ultrasound feasible within the protocol time window (within 6 hours of head CT)

Exclusion criteria

* Open skull fracture * Prior hemicraniectomy * Cranial surgical defect at the insonation site * Anticipated transition to comfort-only care * Any clinical condition in which cranial ultrasound would delay a time-critical intervention

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic accuracy of cranial point-of-care ultrasound (cPOCUS) versus head CTFirst paired CT-cPOCUS assessment (cPOCUS within 6 hours of head CT; Day 1)Diagnostic accuracy of the adjudicated consensus cPOCUS read (index test) for a binary abnormal versus normal head CT (reference standard = attending radiology CT report), reported as sensitivity, specificity, positive predictive value, and negative predictive value, each with 95% confidence intervals, at the first paired CT-cPOCUS assessment. Abnormal scan is defined as presence of any new midline shift, hydrocephalus or parenchymal echogenicity.

Secondary

MeasureTime frameDescription
Inter-reader reliability of cPOCUS interpretationFirst paired assessment; monitored quarterly through study completion (up to 24 months)Agreement between the two blinded expert readers on the binary cPOCUS classification of midline shift, hydrocephalus or parenchymal echogenicity, quantified by Cohen's kappa (prespecified threshold kappa \>= 0.8); observed agreement and Gwet's AC1 reported given anticipated low prevalence.
Per-reader diagnostic accuracy and paired reader comparisonFirst paired CT-cPOCUS assessment (Day 1)Each reader's independent binary cPOCUS call scored against head CT for per-reader sensitivity and specificity for midline shift, hydrocephalus or parenchymal echogenicity ; the two readers compared on the same patients by the paired McNemar test.
Etiology- and subgroup-specific diagnostic accuracy (descriptive)First paired CT-cPOCUS assessment (Day 1)Descriptive, explicitly underpowered estimates of cPOCUS accuracy by prespecified subgroups: age band (2-5, 6-12, 13-17 years), acoustic-window adequacy, mechanism/clinical presentation, and underlying diagnosis; sex-stratified accuracy prespecified per NIH sex-as-a-biological-variable policy.
Age and skull-thickness inflection point (upper age limit of utility)Through study completion (up to 24 months)Identification of the age/skull-thickness threshold above which cranial ultrasound loses screening utility, from age-stratified accuracy and window-adequacy analysis.
Pediatric cPOCUS atlas feature and artifact agreementThrough study completion (up to 24 months)Inter- and intra-observer agreement (Cohen's kappa, age-stratified) on predefined B-mode features and artifacts annotated with a structured ontology, and CT spatial concordance by Horos reformatting/transparency fusion. Atlas and ontology released open access (Zenodo DOI).
Longitudinal midline-shift agreement (cPOCUS vs CT)Serial paired scans over ICU stay (up to 24 months)Agreement between interval change in midline shift (mm) on serial cPOCUS and serial head CT in the CT-positive PICU subset, assessed by Bland-Altman analysis with prespecified limits of agreement.
Longitudinal hydrocephalus and new parenchymal echogenicity agreementSerial paired scans over ICU stay (up to 24 months)Paired concordance between serial cPOCUS and serial head CT for hydrocephalus (present/absent) and new parenchymal echogenicity/new lesion (present/absent), assessed by McNemar's test.
Evolving versus stable pathology (exploratory longitudinal model)Serial paired scans over ICU stay (up to 24 months)Exploratory modeling of evolving versus stable pathology on the subsequent CT using logistic generalized estimating equations (GEE) with robust standard errors (patient as clustering unit); decision-curve analysis for net clinical benefit.

Countries

United States

Contacts

CONTACTAarti Sarwal, MD
aarti.sarwal@vcuhealth.org804-828-9499
PRINCIPAL_INVESTIGATORAarti Sarwal, MD

Virginia Commonwealth University

PRINCIPAL_INVESTIGATORAlia Marie O'Meara, MD

Virginia Commonwealth University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 20, 2026