Enteral Formula Tolerance of Standard Tube Feedings

Completed

Conditions studied: Enteral Feeding

In brief

This prospective observational study seeks to assess ability to achieve enteral feeding goals with standard tube feeding formulas.

Key facts

Study ID

NCT02312271

Run by

Société des Produits Nestlé (SPN)

People needed

102

Starts

2014-12-01

Expected to finish

2017-04-01

Last updated by the study team

2017-05-31

Who can join

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

You may qualify if…

• ≥18 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 21 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)
• Currently participating in another conflicting clinical study that would interfere with anticipated endpoints
• Judged to be at risk for poor compliance to the study protocol.
• Lack of informed consent.

Where it is running

• University of Arkansas — Little Rock, Arkansas, United States
• Vanderbilt University — Nashville, Tennessee, United States
• Bruyere Research Institute — Ottawa, Ontario, Canada

Full record on ClinicalTrials.gov

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