IRCT20210227050510N1RecruitingPhase 3
A comparison of the effect of receiving albumin in the initial 8 to 12 hours and after 24 hours after burn on the incidence of fluid creep in severe burn patients
Rasht University of Medical Sciences0 sites96 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 3
- Status
- Recruiting
- Sponsor
- Enrollment
- 96
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 1 year to no limit (—)
- Sex
- All
Inclusion Criteria
- •burn patients with 2nd and 3rd degree burn area more than 20 percent TBSA
- •full-thickness burn area more than 10 percent TBSA
- •patients needing vasopressor usage in the first 24 hours of admission
- •patients needing intubation and mechanical ventilation in the first 24 hours of admission
Exclusion Criteria
- •patients not needing albumin infusion according to the clinical decision of specialist
- •critically ill patients with expected death in first 24 hours or patients that expired in first 24 hours of admission
- •brain death in first 24 hours
- •patients admitted more than 8 hours after burn
- •patients with chronic underlying diseases affecting serum albumin level, including nephrotic syndrome, cirrhosis, malnutrition, exudative enteropathy
- •a history of cardiac surgery or myocardial infarction in recent 5 years
- •patients with high-voltage electrical burn injuries
- •patient does not accept entering the study
- •patients receiving plasmaphresis
- •a history of reaction to human albumin
Investigators
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