Tolerance of a Calorically Dense Enteral Nutrition Formula

Completed

Conditions studied: Enteral Feeding

In brief

This prospective observational study seeks to demonstrate the ability to meet nutritional needs of a calorically dense enteral formula in critically ill patients.

Key facts

Study ID

NCT02806427

Run by

Société des Produits Nestlé (SPN)

People needed

29

Starts

2016-06-30

Expected to finish

2017-03-11

Last updated by the study team

2017-07-02

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adult aged > 18 years
• Admitted to Medical ICU with expected admission of ≥ 3 days
• Established enteral access
• Having obtained his/her or legal representative's informed consent.

You may not qualify if…

• Pregnant or lactating
• Condition which contraindicates enteral feeding (i.e. intestinal obstruction)
• Lack of enteral access
• Parenteral nutrition
• Any condition that would contraindicate use of the study product (i.e. need for severe fluid restriction, cow's milk protein allergy, etc.)
• Subject who in the Investigator's assessment cannot be expected to comply with study protocol
• Currently participating in another conflicting clinical trial.

Where it is running

• OUHSC — Oklahoma City, Oklahoma, United States

Full record on ClinicalTrials.gov

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