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Feeding Trial in Pediatric Patients

N

Nestlé

Status

Completed

Conditions

Developmental Disabilities

Treatments

Other: enteral formula

Study type

Observational

Funder types

Industry

Identifiers

NCT01469117
11.03.US.HCN

Details and patient eligibility

About

This is a single center, prospective, non-randomized, uncontrolled, observational study of the use of an enteral nutrition product in pediatric patients with developmental disabilities.

Full description

This prospective observational study seeks to assess ability to achieve enteral feeding goals with a new tube feeding product in pediatric patients with developmental disabilities.

Enrollment

16 patients

Sex

All

Ages

1 to 13 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Child aged 1-13 years old with development disabilities
  • Currently tolerating enteral feeding
  • Requiring nutritional management to meet 50-90th% weight for age on the Kennedy Kreiger Growth Charts
  • Requires enteral tube feeding for at least 14 days.

Exclusion criteria

  • Unable to access gastrointestinal tract for feeding via tube
  • Other condition which contraindicates tube feeding

Trial design

16 participants in 1 patient group

Pediatric developmental disabilities
Description:
Children aged 1-13 years old with development disabilities, requiring enteral tube feeding for at least 14 days
Treatment:
Other: enteral formula

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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