Actively Recruiting
Assessment of Nutrient Absorption in Enterally Fed Post-intensive Care Unit Patients Using Bomb Calorimetry: do the Calories Stick
Led by Universitair Ziekenhuis Brussel · Updated on 2026-05-01
20
Participants Needed
2
Research Sites
116 weeks
Total Duration
On this page
Sponsors
U
Universitair Ziekenhuis Brussel
Lead Sponsor
S
Société des Produits Nestlé (SPN)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study focuses on understanding how well patients who have recovered from an ICU stay absorb nutrients when receiving enteral (tube) feeding. Proper nutrition is crucial for recovery, but we don't fully understand how efficiently enteral feeding works in ICU survivors. The study will use advanced techniques like bomb calorimetry to measure the energy content of stool, and indirect calorimetry to measure patients' resting energy expenditure (REE). This will help assess the effectiveness of enteral feeding in these patients, providing valuable information about their metabolic needs and nutritional status. The study will also look into the environmental impact of enteral feeding, particularly food waste. By understanding how much of the nutrition is absorbed versus excreted, the study hopes to suggest more sustainable feeding practices and reduce unnecessary waste in hospitals. Key Goals: * Primary Goal: Measure how much energy from enteral feeding is absorbed by patients post-ICU by analyzing their stool and energy expenditure. * Secondary Goal: Assess how enteral feeding can be made more sustainable, with less waste generated from unused nutritional products. This research will help improve nutritional care for ICU patients, enhance recovery, and potentially lead to more environmentally friendly healthcare practices.
CONDITIONS
Official Title
Assessment of Nutrient Absorption in Enterally Fed Post-intensive Care Unit Patients Using Bomb Calorimetry: do the Calories Stick
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age of 18 years or older
- Minimum ICU stay of 7 days
- Fully dependent on enteral feeding (nasogastric or PEG-tube)
- Ability of the patient or representative to understand and sign written informed consent in Dutch, French, or English
You will not qualify if you...
- Known inflammatory bowel disease
- Known malabsorptive gastrointestinal disease
- History of small bowel resection
- Use of serotoninergic or sympathomimetic medications such as setrone, triptans, antidepressants, methylphenidate, monoamine oxidase inhibitors, or tramadol
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
UZ Brussel
Brussels, Belgium
Not Yet Recruiting
2
UZ Brussel
Jette, Belgium, 1090
Actively Recruiting
Research Team
E
Elisabeth De Waele
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here