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Enteral Formula Tolerance of Standard Tube Feedings

N

Nestlé

Status

Completed

Conditions

Enteral Feeding

Treatments

Other: enteral formula

Study type

Observational

Funder types

Industry

Identifiers

NCT02312271
14.01.US.HCN

Details and patient eligibility

About

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

Enrollment

102 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ≥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.

Exclusion criteria

  • 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.

Trial design

102 participants in 1 patient group

enterally fed adults
Description:
adult subjects with established enteral access receiving standard tube feeding formula
Treatment:
Other: enteral formula

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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