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EPIMix Versus CT Brain Pediatric Study

EPIMix (Echo Planar Imaging Mix) Versus CT Brain Pediatric Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03847051
Enrollment
15
Registered
2019-02-20
Start date
2019-02-15
Completion date
2022-07-30
Last updated
2023-10-17

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

Conditions

Brain Diseases

Keywords

MRI (magnetic resonance imaging), Neuroradiology, EPIMix (Echo planar imaging mix), Multicontrast EPI (echo planar imaging), Clinical validation

Brief summary

This study aims to assess the diagnostic feasibility and diagnostic performance of a new fast MR sequence EPIMix for neuroradiological evaluation in comparison to computed tomography of brain in pediatric population.

Detailed description

The study aims to assess the feasibility of fast MR sequence for neuroradiological evaluation in comparison to computed tomography of brain in pediatric population. Imaging quality is analysed with regards to artefacts and lesion conspicuity as well as its diagnostic potential in rendering a probable diagnosis. The primary study aim is to define feasibility and the AUC for diagnostic performance of minute MRI compared to computed tomography. Included patients are children age 4-18 with suspicion of cerebral pathology with referral to elective computed tomography of the brain. Study participants are in addition to computed tomography investigated during same day at 3T MR.

Interventions

DIAGNOSTIC_TESTMRI

Brain MRI without intravenous contrast

Sponsors

GE Healthcare
CollaboratorINDUSTRY
Karolinska University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Age 4-18 years. * Patient with suspicion of cerebral pathology. * Referral to elective brain CT study.

Exclusion criteria

* CT planned with sedation * known previous cerebral pathology (follow up study) * Emergency CT * Aborted MR exam

Design outcomes

Primary

MeasureTime frameDescription
Tolerance of a new fast MR method in childrenAt 0 hoursNumber of aborted MR
Diagnostic potentialAt 0 hoursDiagnostic accuracy to categorize scan as normal or abnormal on a five point Likert scale (1 - definitely normal, 2 - Probably normal, 3 - Indeterminate, 4 - Probably abnormal, 5 - Definitely abnormal) compared to abnormal/normal brain CT.

Secondary

MeasureTime frameDescription
Diagnostic imaging qualityAt 0 hoursDiagnostic imaging quality (5 point Likert scale; 1 - Excellent diagnostic imaging quality, 2 - Good diagnostic imaging quality, 3 - Sufficient diagnostic imaging quality, 4 - Restricted diagnostic imaging quality, 5 - Poor diagnostic imaging quality)
Lesion descriptionAt 0 hoursFor example effect on brain parenchyma and size
Diagnostic confidenceAt 0 hoursFive point Likert scale (Very confident, Predominantly confident, Fairly confident, Only slightly confident, Not at all confident)
Lesion classificationAt 0 hoursClassification into disease categories (Neoplastic, Ischemic, Hemorrhagic, Infection, Neuroinflammation, Hydrocephalus, Congenital malformation, Indeterminate)
Ability to rule out diseasesAt 0 hoursA list of diseases. Number of positive versus negative cases for each investigation (including: Tumor, Abscess, Parenchymal Haemorrhage, Acute Ischemia, Hydrocephalus, Neuroinflammation, Subarachnoid hemorrhage, Extraaxial fluid collection)
ArtefactsAt 0 hoursArtefacts and impact (Motion, Beam hardening, Other) defined as; Not present, Not affecting diagnostic confidence, Degrading diagnostic confidence)
Clinical diagnostic summary reportAt 0 hoursText (one sentence summary of the finding including type of lesion and location)
Lesion location determinationAt 0 hoursAnatomical localization of abnormality (Cerebrum, Cerebellum, Brainstem, Intraventricular, Subarachnoid space including basal cisterns, Intra-orbital, Skull/Skull base/dural, Other)

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026