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Clinical Trials in the USA / NCT07857070
Starting soon Observational

Newborn Brain Assessment - CergenX Wave

NCT07857070 · tracked via the Priya Life Science USA tracker
Sponsor
CergenX Limited
Phase
Observational
Started
2026-09
Last updated
2026-10-05

Condition(s) studied

Neonatal EncephalopathyNeonatal Encephalopathy (Neonatal Hypoxic-ischemic Encephalopathy)Neonatal Encephalopathy, Unspecified

Investigational drug(s) / intervention(s)

CergenX Wave

CergenX Wave: The amplifier is used to acquire and transmit the EEG to the CergenX Wave software that is installed in a COTS computer.

Study summary

In this study we want to assess how a newly developed software device called CergenX Wave compares to the modified Sarnat examination, performed by the neonatology team . The Wave software algorithm (which is a set of rules used by the computer) analyses EEG activity, using four electrodes placed on the neonate's scalp.

A portable EEG machine records the EEG activity and a tablet will send this information to the cloud where the device analyses the data, as shown in the figure below. The EEG activity the Wave device evaluates will not be available to either the research or clinical team during the investigation but once the recording is completed the device will display a code on screen for the research team to confirm completion.

The results will not be visible to either the researchers or the clinical team therefore will not in any way influence the care of the neonate. This is a regulated observational investigation to compare how the software performs against the current standard of care, a standardised neurological examination.

Eligibility

Sex
ALL
Min age
36 Weeks
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Infants born at ≥36+0 weeks gestational age 2. Informed consent obtained AND 3. A pH of ≤7.0 or base deficit ≥16 (on cord or 1st infant blood gas at \< 1 hour of life) OR 4. a) A pH of 7.01-7.15 or base deficit ≥ 16 (on cord or 1st infant blood gas at \< 1 hour of life) WITH b) at least one of the following: * An APGAR score ≤5 at 10 minutes OR * Prolonged resuscitation (infant receiving IPPV at ≥10 minutes of life) OR * An acute perinatal event: * Abnormal CTG (variable/late foetal HR decelerations) * Foetal bradycardia * Prolapsed/ruptured/tight nuchal cord * Shoulder dystocia * Uterine rupture * Maternal haemorrhage/placental abruption * Maternal trauma (e.g. vehicle accident) * Mother received CPR Exclusion Criteria: 1. Infants \< 36 weeks gestation 2. No parental/guardian consent

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
University of Texas Southwestern Medical Center Dallas Texas
Cork University Maternity Hospital Cork Cork

Other trials for the same condition

Official registry record

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.

View NCT07857070 on ClinicalTrials.gov ↗ ← All trials in the USA