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A Pilot Study of Seizure Detection in Neonates Using Multimodal Temporary Epidermal Electronics
For any newborn that exhibits possible seizure activity or has altered mental status of unknown etiology, continuous bedside EEG recording is the standard of care to detect subclinical seizure activity. The experimental aspect of this study will be the application of test electrodes (EES or EKG) to evaluate if the electrodes can be used to produce a continuous bedside recording of brain activity in the same manner as an EEG recording, while ideally producing less irritation of newborn skin than conventional EEG electrodes.
Infants admitted to our NICU that require a standard EEG for clinical diagnosis will be approached for consent to test one of two new methods of EEG recording. Patients will be randomized to the new epidermal electronic system (EES) or the a hydrogel EKG electrode. All patients will continue to receive the standard of care EEG monitoring. EES is slim new temporary tattoo technology that can easily be applied to the skin without requiring a technician or scrubbing and preparation as with standard EEG lead. The hydrogel EKG are FDA approved leads normally used to detect cardiac rhythm. Specific Aims: 1. To compare the rate of detection of neonatal seizures between a new method of recording electrical brain rhythms (EES or EKG) and the current standard of care (EEG, or electroencephalography.) 2. To compare characterization of electrical brain activity between EES or EKG and EEG in the neonate.
Age
0 - No limit years
Sex
ALL
Healthy Volunteers
No
Sharp Mary Birch Hospital for Women and Newborns
San Diego, California, United States
Start Date
January 27, 2015
Primary Completion Date
November 3, 2017
Last Updated
September 7, 2018
13
ACTUAL participants
Lead Sponsor
Sharp HealthCare
Collaborators
NCT05077904
NCT05667142
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT06448780