Evolution of the Initial Distribution Volume of Glucose in the Severe Burned Adults

Recruiting now · Phase 2

Conditions studied: Burns, Intensive Care, Emergencies

In brief

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.

Key facts

Study ID

NCT06469970

Run by

Centre Hospitalier Régional Metz-Thionville

People needed

15

Starts

2024-11-28

Expected to finish

2027-03-28

Last updated by the study team

2026-03-12

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients over 18 years of age
• Patients hospitalized with burns of at least 30% of body surface area
• By a thermal mechanism
• At the CHR Metz-Thionville burn center
• managed within the 8 hours post-burn
• Patient affiliated to a social security scheme
• Written consent obtained from the patient (or from the trusted person, family or relatives if the patient is unable to sign/express consent) or emergency inclusion if the patient is unable to express consent and neither the trusted support person nor any member of the family or relatives is present at the time of inclusion.

You may not qualify if…

• Diabetic patients on insulin
• Patient with a CONTRAINDICATION to GLUCOSE 30% PROAMP, solution for injection
• Patients with pre-hospital cardiac arrest
• extra corporeal circulation patient: Extra Corporeal Membranous Oxygenation (ECMO) or Extra Corporeal Life Support (ECLS) or CRRT (Continuous Renal Replacement Therapy)
• patient without a central venous line or arterial catheter
• Patient moribund or immediately subject to therapeutic limitation
• Impossibility of trans-pulmonary thermodilution monitoring (vascular access difficulties)
• Pregnant, parturient or breast-feeding women
• Patient under guardianship, curatorship or safeguard of justice
• Cognitive impairment or language barrier

Where it is running

• CHR Metz-Thionville/Hopital de Mercy — Metz, France (enrolling)

Full record on ClinicalTrials.gov

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