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Study identifier: NCT06726408 Synced from ClinicalTrials.gov · July 28, 2026
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Critical Care Optimized Pediatric and Neonatal Quantitative Neuromonitoring

Condition: Neonatal Intensive Care Unit  ·  Sponsor: Nantes University Hospital

PhaseN/A
Planned participants120
Who can joinAll sexes, N/A to 24 Months
Healthy volunteersNo

About this study

The detection and appropriate treatment of seizures significantly impact the neurological prognosis of patients in intensive care. Indeed, altered brain function including seizures is described in critically ill children, regardless of the reason for admission. Most seizures are subclinical and therefore impossible to diagnose without neuromonitoring tools. Despite being concidered ad Gold Standard, continuous EEG (cEEG) with video recording shows difficulty of implementation and interpretation at all hours of the day and night explaining that less than 10% of centers in France use cEEG routinely. Most departments prefer simplified techniques, including amplitude traces (aEEG) which can be used continuously at the bedside. However, the positive predictive value of aEEG in the detection of seizures does not exceed 78% and 64% in newborns and children respectively making necessary an optimization of the information provided by these techniques. This project is a pragmatic diagnostic study that aims at developing and evaluating a neuromonitoring interface adapted to the needs of pediatric and neonatal intensive care units and meeting the requirements of neurophysiologists in terms of EEG trace quality.

This description comes directly from the study's public registry record.

Talk to the study team

Noura ZAYAT, PH  ·  33 2 76 64 37 91  ·  noura.zayat@chu-nantes.fr

Pierre BOURGOIN, PH  ·  33 2 76 64 36 12  ·  pierre.bourgoin@chu-nantes.fr

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Locations (1)

CHU de NantesNantes, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06726408