Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06023251

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

Led by Universitair Ziekenhuis Brussel · Updated on 2024-03-26

100

Participants Needed

1

Research Sites

151 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult 18 years or older
  • ICU stay of 7 days or more
  • Ward stay of 3 days or more
  • No restrictions on nutritional therapy
  • Patients with various underlying diseases
Not Eligible

You will not qualify if you...

  • Patients younger than 18 years
  • ICU stay less than 7 days
  • Ward stay less than 3 days
  • Advanced care planning affecting nutritional therapy
  • Receiving palliative care
  • Metabolic diseases or metabolic derangements
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UZ Brussel

Brussels, Belgium

Actively Recruiting

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Research Team

Z

Zenzi Rosseel, PharmD

CONTACT

L

Lotte Buyle, RD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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