Actively Recruiting

Phase 2
Phase 3
Age: 39Weeks - 54Weeks
All Genders
NCT07049952

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

Age: 39Weeks - 54Weeks
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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

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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

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