- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04500483
Indirect Calorimetry in Patients at Risk of Malnutrition
June 25, 2023 updated by: Anne-Françoise Rousseau, University of Liege
Measurement of Resting Energy Expenditure in Burn or Critically Ill Patients at Risk of Malnutrition
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.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Anne-Françoise Rousseau, MD, PhD
- Phone Number: +3243667495
- Email: afrousseau@chuliege.be
Study Locations
-
-
-
Liège, Belgium, 4000
- Recruiting
- University Hospital of Liege
-
Contact:
- Anne-Françoise Rousseau, PhD
- Phone Number: +3243667495
- Email: afrousseau@chuliege.be
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
the study population is divided into two groups: burn patients with minor burn exclusively treated in an outpatient setting, and ICU survivors who were discharged fro ICU after a stay of at least 7 days
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Burn outpatients
Burn patients treated for minor burns in an outpatient setting
|
measurement of resting energy expenditure using indirect calorimetry
|
ICU survivors
Critically ill patients who survived ICU stay and are admitted in a general ward
|
measurement of resting energy expenditure using indirect calorimetry
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
resting energy expenditure
Time Frame: during the 7 days following injury in burn patients or following ICU discharge in ICU survivors
|
during the 7 days following injury in burn patients or following ICU discharge in ICU survivors
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 15, 2020
Primary Completion (Estimated)
August 15, 2023
Study Completion (Estimated)
August 15, 2025
Study Registration Dates
First Submitted
August 1, 2020
First Submitted That Met QC Criteria
August 1, 2020
First Posted (Actual)
August 5, 2020
Study Record Updates
Last Update Posted (Actual)
June 27, 2023
Last Update Submitted That Met QC Criteria
June 25, 2023
Last Verified
June 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CaloIF
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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