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.
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.
Study Type
OBSERVATIONAL
Enrollment
16
Complete feeding of study enteral formula, route and regimen prescribed by the physician
The Children's Center
Bethany, Oklahoma, United States
Time to feeding goal achievement
Time frame: up to 14 days
Gastrointestinal measures assessment
Time frame: up to 21 days
Percentage of nutrition goal met
Time frame: daily up to 21 days
Serum biochemical markers assessment
Time frame: baseline and completion of study
Assessment of frequency and nature of adverse events
Time frame: daily up to 21 days
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