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Tube Feeding Tolerance After Switch to Peptide Based Formula in Children With Developmental Delay

N

Nestlé

Status

Completed

Conditions

Developmental Disabilities
Feeding Disorder

Study type

Observational

Funder types

Industry

Identifiers

NCT02912065
14.08.US.HCN

Details and patient eligibility

About

A retrospective chart review to assess feeding tolerance in children who had been switched from an intact protein formula to a Peptide based formula due to feeding intolerance in a pediatric facility for the developmentally delayed.

Full description

Medical records of pediatric patients with enteral feeding intolerance on standard polymeric formulas that were switched to a peptide based formula will be retrospectively analyzed. Data will be collected on caloric intake, ability to meet enteral nutrition goals, incidence of intolerance, and the use of medications to control gastrointestinal symptoms.

Enrollment

13 patients

Sex

All

Ages

13 months to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 13 months to < 18 years of age on admission to facility
  • Required enteral nutrition to meet 90% or more of their energy needs prior to switch to a Peptide based formula
  • Received enteral nutrition with an intact protein formula for a minimum of two weeks prior to a switch to a Peptide based formula
  • Have documentation of intolerance to an intact protein formula, followed by a switch in formula received to a Peptide based formula
  • Have documentation of an assessment of feeding tolerance following the switch to a Peptide based formula
  • Formulas received must be indicated for use in children or adults (not infant formulas).

Exclusion criteria

  • Recent abdominal surgery, change in tube position/placement (within past 30 days)
  • Cow's milk protein allergy
  • Any current infections including upper respiratory, viral, gastroenteritis, wound infection.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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