Actively Recruiting

Phase 3
Age: 18Years - 80Years
All Genders
NCT06968559

Effect of Early Dexamethasone on Major Complications and All-cause Mortality in Severe Burns

Led by Nantes University Hospital · Updated on 2025-11-18

478

Participants Needed

10

Research Sites

169 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Burns affect more than 11 million people worldwide each year. These injuries are responsible for severe morbidity resulting in a high societal burden and account for more than 180,000 yearly deaths especially in low- and middle-income countries. Major burns induce an important local and systemic inflammatory response that may be overwhelmed. This inflammation is a physiological phenomenon that favours the healing of tissues. However, the overproduction of inflammatory mediators might lead to an exacerbated Systemic Inflammatory Response Syndrome (SIRS). Recently the total body surface area (TBSA) burned has shown to be well correlated to persistent elevation of pro-inflammatory mediators (such as IL-6). This SIRS, in turn, contributes to the enhanced risk of sepsis, acute respiratory distress syndromes (ARDS) and organ failures in general such as acute kidney injuries (AKI), most of those occurring within the first week of admission. Corticosteroids (CS) have already proven their effectiveness against SIRS-induced organ dysfunction or mortality in acute medicine notably in septic shock, polytraumatized patients and more recently in the treatment of viral or non-viral ARDS without increasing the risk of secondary bacterial complications or significant side effects . Indeed the recent SCCM Guidelines clearly advocate for the use of CS in severe community-acquired pneumonia, septic shock and ARDS. The investigators recently performed a large multicenter, double-blinded randomized controlled trial (the PACMAN trial, PHRC-N 2016) including 1222 patients scheduled for major surgery in which the investigators observed a major decrease in CRP blood concentrations in the dexamethasone arm. The rate of AKI and the need for mechanical ventilation were also significantly reduced in the intervention arm. ICU Patients with severe burns undergo several surgeries, including major procedures (excision, skin grafts), rendering them quite similar to those in the PACMAN trial in terms of inflammatory response. Very few side effects (hyperglycemia mainly) easily overcome in ICU are usually reported with the use of low-to-moderate dose of CS. In severe burn patients, very few data are available to date, two retrospective case control studies and a small prospective randomized trial showed promising results when using CS but high quality evidence is lacking. The investigators hypothesise here that the use of dexamethasone after major burns, the prototypic model of inflammatory response in surgical ICU patients, would limit SIRS-induced organ failure and/or all-cause mortality.

CONDITIONS

Official Title

Effect of Early Dexamethasone on Major Complications and All-cause Mortality in Severe Burns

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 80 years old
  • Total burn surface area of 20% or more, measured by a trained expert
  • Receiving invasive mechanical ventilation at the time of inclusion
  • Burn injury occurred within the last 48 hours
  • Informed consent provided by next-of-kin, legal representative, or emergency procedure
  • Affiliated with or beneficiary of the French social security system
Not Eligible

You will not qualify if you...

  • Imminent death with a do-not-resuscitate order
  • History of hypersensitivity to dexamethasone or its ingredients
  • Pregnancy or breastfeeding (confirmed by pregnancy test for women of childbearing age)
  • Participation in another drug study with known interactions with dexamethasone
  • Uncontrolled viral hepatitis or invasive fungal infection at inclusion
  • Prolonged steroid use in the last 90 days (more than 0.3 mg/kg/day prednisolone equivalent)
  • Moderate-to-severe acute respiratory distress syndrome upon admission

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 10 locations

1

CHU Tours

Chambray-lès-Tours, France, 37170

Not Yet Recruiting

2

CHU Lille

Lille, France, 59037

Not Yet Recruiting

3

CHU de Lyon

Lyon, France, 69437

Not Yet Recruiting

4

Aphm Hopital La Timone

Marseille, France, 13005

Not Yet Recruiting

5

CHR Metz

Metz, France, 57085

Not Yet Recruiting

6

CHU Montpellier

Montpellier, France, 34295

Not Yet Recruiting

7

Chu Nantes

Nantes, France, 44093

Actively Recruiting

8

HU Saint-Louis Lariboisière

Paris, France, 75475

Not Yet Recruiting

9

CHU Bordeaux

Pessac, France, 33604

Not Yet Recruiting

10

CHU Toulouse

Toulouse, France, 31059

Not Yet Recruiting

Loading map...

Research Team

K

Karim ASHENOUNE, MD, PhD

CONTACT

A

Alexandre BOURDIOL, PH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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