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Recruiting Observational

Albumin and Prognosis of Severely Patients Burns

NCT04264065 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2022-09-16
Last updated
2026-01-15

Condition(s) studied

Severe Burn

Study summary

Hemodynamic management has long been identified as a key factor affecting burn prognosis. However, large amounts of crystalloid infusion have been associated with the development or aggravation of organ failure (acute respiratory distress syndrome, vascular injury, acute renal failure, and intra-abdominal hypertension) which worsens the final prognosis.

The use of albumin during the first 24 hours of burn resuscitation is controversial since capillary leakage may cause transcapillary passage of large molecules into the interstitial space. In fact, human albumin has multiple physiological effects, including regulation of colloidal osmotic pressure, antioxidant properties, nitric oxide modulation and buffering capacities, plasma binding and transport of various substances, which may be particularly important in severe burns.

Currently available data suggest that administration of exogenous albumin during the first 24 hours of resuscitation of severe burn patients may be associated with improved outcomes. Multi-centre randomized controlled trials with adequate power should be undertaken in burned patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Patients over 18 years of age * Burns \> 30% SCT * Patients admitted to the ICU within 12 hours of a burn. Exclusion Criteria: * Pregnancy * Patients with a limitation of active therapeutics on admission to BICU * Pre-hospital cardiac arrest * Moribund patients: pre-hospital cardiac arrest, CBS burn \>95%. * Age \>80 years

Primary outcome measure(s)

  • The primary endpoint will be a combined endpoint of mortality, stage 3 acute renal failure and severe acute respiratory distress syndrome within 28 days of burn injury. — 28 days of burn injury

Trial sites (1)

FacilityCityRegionStatus
Hopital saint Louis Paris France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04264065 on ClinicalTrials.gov ↗ ← All trials in France