Time PerceptionRhythmEEGfNIRSERPPremature NeonatesDiscrimination
Investigational drug(s) / intervention(s)
EEGNIRS
EEG: EEG recording during prematurity or around term
NIRS: NIRS recording during prematurity or around term
Study summary
Premature neonates are able to discriminate phonemes and voice from 28wGA at a time the neuronal network establish contact between the environment and the cortical neurones. In the present monocentric study the investigators will analyse the response of the cortical network in premature aged between 28 and 40 wGA in response to auditory stimuli using High Resolution Electroencephalography and High Density Near Infrared Spectroscopy
Eligibility
Sex
ALL
Min age
0 Days
Max age
18 Years
Healthy volunteers
No
Inclusion Criteria:
* Full term neonates between 28 and 40 weeks Gestational Age
Exclusion Criteria:
* Neonates outside the age range
Primary outcome measure(s)
Variations of the response of the cortical network using High Resolution Electroencephalography before auditory stimuli between the 5 infant groups — one day
Variations of the response of the cortical network using High Resolution Electroencephalography during auditory stimuli between the 5 infant groups — one day
Variations of the response of the cortical network using High Resolution Electroencephalography after auditory stimuli between the 5 infant groups — one day
variations of the response of the cortical network using High Density Near Infrared Spectroscopy before auditory stimuli between the 5 infant groups — one day
variations of the response of the cortical network using High Density Near Infrared Spectroscopy during auditory stimuli between the 5 infant groups — one day
variations of the response of the cortical network using High Density Near Infrared Spectroscopy after auditory stimuli between the 5 infant groups — one day
Trial sites (1)
Facility
City
Region
Status
CHU Amiens
Amiens
France
Recruiting
More Centre Hospitalier Universitaire, Amiens trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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