Clinical Trial

Improving Nutritional Adequacy of ICU Survivors in a Prospective Interventional Way: the Bright Side Study

Study acronym: BrightSide
Recruiting
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Summary
The objective is to increase caloric adequacy in patients who survived critical illness and are admitted to the ward by the use of a pro-active inclusive nutritional strategy including supplemental parenteral and/or enteral nutrition and/or oral nutritional supplements guided by indirect calorimetry. This enables the investigators to address, within a clinical/scientific context, a recently demonstrated but until now relatively neglected 'dark side' of patient care at UZ Brussel, comparable to limited global evidence : iatrogenic malnutrition of ICU survivors. The use of a newly developed clinical pathway and nutrition strategy (oral, enteral and parenteral) led by a single SPoC (Single Point of Contact) for patients surviving intensive care will have a clear objective: to address the nutritional deficit in all patients.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2023-09-01.
Status change: Not Yet Recruiting → Recruiting 2024-03-22
Trial Details
NCT Number NCT06023251
Lead Sponsor Universitair Ziekenhuis Brussel
Conditions Malnutrition
Enrollment 100 participants
Start Date 2023-10-04
Primary Completion 2026-08-31 (estimated)
Study Completion 2026-08-31 (estimated)
Updated on ClinicalTrials.gov 2024-03-26