Tolerance of a Calorically Dense Enteral Nutrition Formula
Completed
- Conditions
- Enteral Feeding
- Registration Number
- NCT02806427
- Lead Sponsor
- Société des Produits Nestlé (SPN)
- Brief Summary
This prospective observational study seeks to demonstrate the ability to meet nutritional needs of a calorically dense enteral formula in critically ill patients.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 29
Inclusion Criteria
- 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.
Exclusion Criteria
- 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.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Daily percentage of caloric nutritional goal met First 3 days in the ICU
- Secondary Outcome Measures
Name Time Method Daily percentage of protein goal met First 5 days in the ICU Adverse events and serious adverse events First 5 days in the ICU
Trial Locations
- Locations (1)
OUHSC
🇺🇸Oklahoma City, Oklahoma, United States
OUHSC🇺🇸Oklahoma City, Oklahoma, United States