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NCT04500483 Clinical Trial

Indirect Calorimetry in Patients at Risk of Malnutrition

Critical Illness Clinical Trial

Official title:
Measurement of Resting Energy Expenditure in Burn or Critically Ill Patients at Risk of Malnutrition

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04500483
Other study ID # CaloIF
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 15, 2020
Est. completion date August 15, 2025

Study information
Verified date June 2023
Source University of Liege
Contact Anne-Françoise Rousseau, MD, PhD
Phone +3243667495
Email afrousseau@chuliege.be
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Burn patients treated in an outpatient clinic and ICU survivors are at risk of malnutrition. There are no clear guidelines determining the energy target in those two populations. The aim of this observation study is to measure the resting energy expenditure of those patients, using indirect calorimetry.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date August 15, 2025
Est. primary completion date August 15, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - minor burn treated in an outpatient setting - ICU survivor, who was discharged from ICU after a stay of at least 7 days Exclusion Criteria: - oxygen supply - chest drainage - not french speaking - confusion, coma - cognitive disorder - patient refusal

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• indirect calorimetry
measurement of resting energy expenditure using indirect calorimetry

Locations
Country Name City State
Belgium University Hospital of Liège Liège

Sponsors (1)
Lead Sponsor Collaborator
University of Liege

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary resting energy expenditure during the 7 days following injury in burn patients or following ICU discharge in ICU survivors
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