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An evaluation of the effect of albumin administration time on the incidence of fluid creep in severe burn patients

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

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210227050510N1
Enrollment
96
Registered
2021-07-13
Start date
2021-07-23
Completion date
Unknown
Last updated
2021-08-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burn. Burns classified according to extent of body surface involved

Interventions

Intervention 1: Intervention group: The intervention group will receive 20% human albumin 0.125 milliliters per kilogram body weight per percent body surface burn between 8 to 12 hours after admission

Sponsors

Rasht University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to No maximum

Inclusion criteria

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

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 pregnancy 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

Design outcomes

Primary

MeasureTime frame
Fluid creep, patient's fluid intake exceeding estimated intake with parkland formula. Timepoint: 12 hours and 1,2,3,5, and 7 days after-burn. Method of measurement: assessment of the fluid intake of patient to maintain a satisfactory urine output.

Secondary

MeasureTime frame
Length of hospital stay. Timepoint: At the time of hospital discharge. Method of measurement: Days.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadreza Mobayen

Rasht University of Medical Sciences

mmobayen@gums.ac.ir+98 13 3336 9633

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026