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

Recruiting N/A Interventional Study
Malnutrition
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
100 (estimated)
Sponsor
Universitair Ziekenhuis Brussel · Other
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About This Trial
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 demon…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adult ≥ 18 years * ICU stay ≥ 7 days * Ward stay ≥ 3 days * Nutritional therapy not restricted * Heterogeneous diseases Exclusion Criteria: * Patients \< 18 years * ICU \< 7 days * Ward stay \< 3 days * Advanced Care Planning with impact on nutritional therapy * Patients wit…
Contacts

Zenzi Rosseel, PharmD

003224763344

zenzi.rosseel@uzbrussel.be

CONTACT

Lotte Buyle, RD

003224763344

lotte.buyle@uzbrussel.be

CONTACT