Enteral Formula Tolerance in Pediatric Patients

Completed · Not applicable

Conditions studied: Enteral Nutrition

In brief

The purpose of this prospective study seeks to assess ability to achieve enteral feeding goals with standard polymeric enteral formula in a stable, pediatric tube-fed population.

Key facts

Study ID

NCT02779335

Run by

Société des Produits Nestlé (SPN)

People needed

22

Starts

2016-05-01

Expected to finish

2016-10-01

Last updated by the study team

2016-10-21

Who can join

Age: 1 and older, up to 13. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 1 - 13 years of age
• Currently tolerating enteral feeding
• Has enteral access
• Requires enteral tube feeding to provide 90% or more of their nutritional needs (without the use of modular(s)) for at least 9 days
• Having obtained his/her and/or his/her legal representative's informed consent

You may not qualify if…

• Condition which contraindicates enteral feeding (i.e. intestinal obstruction)
• Lack of enteral access
• Any condition that would contraindicate use of the study product (i.e. need for severe fluid restriction, cow's milk protein allergy, other)
• Judged to be at risk for poor compliance to the study protocol
• Lack of informed consent
• Currently participating in another conflicting clinical trial

Where it is running

• Children's Center for GI and Nutrition — Hollywood, Florida, United States

Full record on ClinicalTrials.gov

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