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Prognostic Value of Arterial Spin Labeling Brain Perfusion MRI in Term Neonates With Hypoxic-ischemic Encephalopathy

Prognostic Value of Arterial Spin Labeling Brain Perfusion MRI in Term Neonates With Hypoxic-ischemic Encephalopathy

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04325230
Acronym
BBASL
Enrollment
31
Registered
2020-03-27
Start date
2020-05-17
Completion date
2023-01-12
Last updated
2026-05-29

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

Conditions

Neonatal Hypoxic Ischemic Encephalopathy

Keywords

Hypoxic-ischemic encephalopathy, Neonate, Perfusion, MRI, Arterial Spin Labeling

Brief summary

The main purpose of this study will be to evaluate the prognostic value at 3 months of life of brain perfusion MRI determined by Arterial Spin Labeling technique in the first week of life of term newborns with hypoxic-ischemic encephalopathy requiring management in neonatal intensive care unit.

Detailed description

Hypoxic-ischemic encephalopathy is the result of birth asphyxia due to transitory cerebral blood flow drop during perinatal period. It is the leading cause of neonatal encephalopathy, and thus a major cause of perinatal mortality, morbidity and adverse neurodevelopmental outcome. Usual care brain MRI is critically important in the diagnosis and prognosis. Lasting about 30 to 40 minutes, MRI exam includes successive sequences providing complementary information but none relatively to brain perfusion. Perfusion MRI without contrast media injection is possible using Arterial Spin Labeling (ASL) sequence. ASL is highly suitable for neonates, noninvasiveness, and lasts only 5 minutes. However, only one study assessed ASL as a prognostic factor. The purpose of the study is therefore to perform ASL sequence within usual care brain MRI.

Interventions

DEVICEArterial Spin Labeling sequence

ASL sequence added to the usual care brain MRI

Sponsors

University Hospital, Bordeaux
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Days to 8 Days
Healthy volunteers
No

Inclusion criteria

* neonates with a term ≥ 36 weeks of amenorrhea and birth weight ≥ 1800 g. * presenting with perinatal asphyxia defined as combination of: * an acute perinatal event (such as placental abruption, cord prolapse, and/or severe foetal heart rate abnormalities); * and at least one of the following criteria: * Apgar score ≤ 5 at 10 minutes of life, * mask ventilation or intubation at 10 minutes of life, * metabolic acidosis defined as pH \< 7 or base deficit ≥ 16 mmol/L or lactates ≥ 11 mmol/L within the first 60 minutes of life on cord or other arterial venous or capillary blood sample. * patient treated or not with therapeutic hypothermia for 72 hours. * affiliated patient or beneficiary of a social security scheme. * informed and signed parental consent.

Exclusion criteria

* perinatal arterial ischemic stroke. * congenital neuro-metabolic disorder. * severe malformative abnormalities. * MRI contra-indication. * Poor understanding of the holders of parental authority

Design outcomes

Primary

MeasureTime frameDescription
Clinical outcome3 months of life (Month 3)judged as favorable, or as adverse in case of death or cerebral palsy

Secondary

MeasureTime frameDescription
Clinical outcomeMonth 6, Month 12judged as favorable or as adverse
Prognostic performances of ASLBaselinePrognostic performances of ASL in comparison with routinely used MRI parameters
Quality of ASL sequencesBaselineaccording to visual analysis of artifacts and number of negative voxels
Inter-observer agreement of the interpretation of the perfusion dataBaselineIntra Class correlation coefficient

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 30, 2026