utritional support algorithm for critically ill patients

Not Applicable

Completed

• Conditions: Enteral feeding; Nutritional, Metabolic, Endocrine

• Registration Number: ISRCTN10583582
• Lead Sponsor: Zhejiang Provincial People's Hospital

Brief Summary

2016 Protocol article in http://www.ncbi.nlm.nih.gov/pubmed/27668228 protocol 2017 Results article in https://www.ncbi.nlm.nih.gov/pubmed/28771622 results

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-05-26
• Study Completion: 2016-12-18
• Last Update Posted: 26 June 2023

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 350

Inclusion Criteria

Critically ill patients expected to stay in ICU for more than 3 days

Exclusion Criteria

1. Previous EN within 7 days of current episode of ICU admission
2. Burn patients
3. Pregnancy and breast feeding
4. Patients with PEJ, PEG

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
28-day mortality

Secondary Outcome Measures

Name	Time	Method
1. Incidence of ventilator associated pneumonia<br>2. Length of stay in ICU and hospital<br>3. Duration of mechanical ventilation<br>4. Biomarkers of nutritional status, including albumin, pre-albumin, chemistry profile, CD3, CD8, IgA, IgG, HLA-DR. They are measured via blood samples taken on a daily basis after enrollment into the study<br>5. Total amount of nutrition and the proportions of enteral and parenteral nutrition, measured by summing up calories intakes for the whole study period. Calories include enteral nutrition (commercial formula with fixed calorie per unit volume), and parenteral nutrition