Actively Recruiting
BabySTrong II taVNS Feeding Trial
Led by Medical University of South Carolina · Updated on 2025-11-21
88
Participants Needed
1
Research Sites
110 weeks
Total Duration
On this page
Sponsors
M
Medical University of South Carolina
Lead Sponsor
E
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The long-term goal of this project is to develop a therapy to assist pre-term and term infants with brain injury overcome difficulties in learning to feed so that infants may be discharged home with their families and avoid the burdens of of a gastrostomy tube (G-tube) or prolonged home nasogastric feeding. Few other therapies exist for infants who are not making progress with feeding volumes at term age. To tackle this problem, we took the novel approach of pairing non-invasive nerve stimulation of the vagus nerve at the ear (taVNS) stimulation with the motor skills of feeding. In our pilot studies, 54% (19 out of 35) infants with feeding delays whose families were in discussions for G-tube placement, reached full oral feeds within 2 weeks, and infants who did not reach full feeds still improved their daily oral feeding volumes. Infants who got to full feeds showed stronger and more complex brain circuits associated with feeding motor skills. With this trial we will test the BabySTrong taVNS feeding system in a multicenter, randomized, controlled, blinded trial to show how well this feeding system works in improving the daily feeding volumes, the days to full oral feeds, and/or the number of infants who avoid G-tube/ home NG placement, and increasing connections in brain circuits. If this groundbreaking new approach to infant feeding is successful, we may decrease how long infants are in the hospital, costs with Gtubes and home NG feeds, and family and care provider burdens. The findings from this proposal will be used in our FDA application for the BabySTrong feeding system.
CONDITIONS
Official Title
BabySTrong II taVNS Feeding Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Infants older than 39 weeks postmenstrual age (PMA) making minimal progress with oral feeds
- Infants trying to learn feeding for at least 2 weeks if starting feeds at or after 37 weeks PMA
- Infants trying to learn feeding for at least 4 weeks if starting feeds before 36 weeks PMA
- Infants able to take oral feeds every feeding without volume restrictions by therapists
You will not qualify if you...
- Infants with cardiomyopathy
- Infants with unstable apnea or bradycardia
- Infants requiring significant respiratory support such as CPAP or Vapotherm
- Infants with unrepaired major congenital anomalies affecting safe oral feeding or imposing volume limits
- Infants with congenital syndromes unlikely to feed orally
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Shawn Jenkins Children's Hospital, Medical University of South Carolina
Charleston, South Carolina, United States, 29425
Actively Recruiting
Research Team
D
Dorothea D Jenkins, MD
CONTACT
G
Gary Connor, RN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
4
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here