Actively Recruiting
Evolution of the Initial Distribution Volume of Glucose in the Severe Burned Adults
Led by Centre Hospitalier Régional Metz-Thionville · Updated on 2026-03-12
15
Participants Needed
1
Research Sites
121 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a prospective, observational, monocentric, phase II (exploratory) cohort study aiming to describe the evolutionary profile of the initial volume of glucose distribution (IDVG) during the first four days of management of severely burned patient.
CONDITIONS
Official Title
Evolution of the Initial Distribution Volume of Glucose in the Severe Burned Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients over 18 years of age
- Patients hospitalized with burns of at least 30% of body surface area
- Burns caused by a thermal mechanism
- Patients treated at the CHR Metz-Thionville burn center
- Patients managed within 8 hours after the burn injury
- Patient affiliated with a social security scheme
- Written consent obtained from the patient or authorized representative, or emergency inclusion if consent cannot be obtained
You will not qualify if you...
- Diabetic patients on insulin
- Patients with contraindications to Glucose 30% Proamp injection
- Patients who had cardiac arrest before hospital arrival
- Patients undergoing extracorporeal circulation (ECMO, ECLS) or continuous renal replacement therapy (CRRT)
- Patients without a central venous line or arterial catheter
- Moribund patients or those with immediate therapeutic limitations
- Patients unable to undergo trans-pulmonary thermodilution monitoring due to vascular access issues
- Pregnant, parturient, or breastfeeding women
- Patients under guardianship, curatorship, or legal protection
- Patients with cognitive impairments or language barriers
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CHR Metz-Thionville/Hopital de Mercy
Metz, France, 57085
Actively Recruiting
Research Team
A
Arpiné EL NAR, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here