Burn. Burn and corrosion of head, face, and neck
Conditions
Interventions
Intervention 1: Intervention group: recipient of mitomycin C with a concentration of .4 mg/d, one dose, manufactured by KOREA UNITED PHARM. Intervention 2: Control group: Control group: triamcilonone,
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with burns and needing injections Patients over 18 years old
Exclusion criteria
Exclusion criteria: • Pregnant women and nursing mothers • People with mental problems • Inability to write or read Farsi • Prisoners • People who do not want to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hypertrophic scars. Timepoint: In a period of 2 months at the beginning of the study and 2 months after the injection. Method of measurement: Measurement is done with a ruler. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAbdulreza Sheikhi
Ahvaz University of Medical Sciences
Outcome results
None listed