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epinephrine and hemostat powder in burn

Comparing the effectiveness of epinephrine and hemostat powder on the prevention of bleeding during burn debridement

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230517058217N1
Enrollment
108
Registered
2023-06-01
Start date
2023-09-23
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Burn. burn

Interventions

Intervention 1: Intervention group: Hemostat powder. Intervention 2: Control group: Diluted epinephrine.

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Thermal burn patients with total body surface area (TBSA) involvement less than 30%

Exclusion criteria

Exclusion criteria: Coagulopathies Active malignancies Autoimmune diseases Patients who receive corticosteroids daily

Design outcomes

Primary

MeasureTime frame
Hemoglobin drop rate. Timepoint: Six hours before surgery and six hours after surgery. Method of measurement: Venous sampling from the brachial vein.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohamad Sabouri

Zanjan University of Medical Sciences

dr.m.sabourii@gmail.com+98 21 8806 4148

Outcome results

None listed

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