Prospective data collection using the Neoneur Feeding System to demonstrate device functionality, correlation to historic data, and prepare for a more extensive phase II SBIR trial
The consented infant's assigned Speech Language Pathologist will use the Neoneur Feeding System 2-3 times a week from initiation of oral feeding until discharge, if oral feeding is prescribed. It can be used either as a special consult, or during routine care. The feeding is performed by the Speech Language Pathologist assigned to the infant. There will be no change in the infant's feeding plan. For infants consented to participate in the study, their feeding will include the Neoneur feeding system inserted between the nipple and bottle. When the Neoneur is inserted, it will capture both the suck and swallow changes (oral cavity pressure), and respiration (temperature changes) patterns.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
100
Feeding Evaluation with Device
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
RECRUITINGMaturation
Neoneur 200 measures are corelated to infant maturation in gestational age
Time frame: 6 weeks of data collection
Telehealth functionality
Evaluation of Sending Neoneur 200 data from the bedside to the cloud for used in the hospital and home
Time frame: 6 months
Respiratory
The evaluation of Neoneur 200's respiratory sensor to collect accurate data
Time frame: 6 months
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