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Improvement Project To Optimizing Nutrition With Higher Protein and Calorie Pediatric Tube Feeding

An Improvement Project Towards Optimizing Nutrition Intervention With a Higher Protein and Calorie Pediatric Tube Feeding Formula

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03017664
Enrollment
28
Registered
2017-01-11
Start date
2018-01-15
Completion date
2019-12-31
Last updated
2020-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Critically Ill Children

Brief summary

This quality improvement project will include a practice change based on national guidelines for the nutritional management of PICU patients.

Detailed description

This quality improvement project will include a practice change based on national guidelines for the nutritional management of PICU patients. The primary aim of this quality improvement project is to better meet protein needs of ICU critically ill children

Interventions

OTHERPeptide-based enteral formula

Peptide-based, higher protein and higher calorie enteral formula

OTHERRetrospective review of enteral tube feeding formula

Enteral formula tube feeding will be retrospectively reviewed

Sponsors

Société des Produits Nestlé (SPN)
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Years to 13 Years
Healthy volunteers
No

Inclusion criteria

* Children aged 1-18 years old with enteral feeding access and anticipated to be fed for 5 days

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Enteral formula volume5 daysDaily total formula volume (mL) delivered

Other

MeasureTime frameDescription
Enteral feeding interruptions5 daysyes/no; if yes, reason for interruption
Diarrhea5 daysyes/no; if yes, frequency in 24 hour period
Protein modular5 daysyes/no; if yes, dose (g/mL) and schedule
Elevated gastric residuals5 daysyes/no; if yes, amount (mL) in 24 hour period
Abdominal distention/pain5 daysyes/no
Vomiting5 daysyes/no; if yes, frequency in 24 hour period

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026