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Feeding Trial in Pediatric Patients

NCT01469117 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 16

Last updated 2014-08-07

No results posted yet for this study

Summary

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.

Conditions

  • Developmental Disabilities

Interventions

OTHER

enteral formula

Complete feeding of study enteral formula, route and regimen prescribed by the physician

Sponsors & Collaborators

  • Société des Produits Nestlé (SPN)

    lead INDUSTRY

Principal Investigators

  • Darin Brannan, MD · The Children's Center

Eligibility

Min Age
1 Year
Max Age
13 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-11-30
Primary Completion
2013-01-31
Completion
2013-01-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01469117 on ClinicalTrials.gov