Burn injury. Burn and corrosion, body region unspecified
Conditions
Interventions
Intervention 1: Intervention group: Calcipotriol ointment 0.005% (Tehran Shimi Company) will be applied topically on the donor site every other day for 10 days. Intervention 2: Control group: No inter
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients undergo split thickness skin graft Patients sign informed consent form
Exclusion criteria
Exclusion criteria: Infection of the donor site Bleeding of the donor site Pregnancy Lactation Hypercalcemia Hyperphosphatemia Renal failure Hepatic impairment Sepsis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percent of epithelialization of the donor site. Timepoint: 10 days after the intervention. Method of measurement: Calculation of the ratio of the surface area of the epithelialized parts to the total surface area of the donor site. | — |
Secondary
| Measure | Time frame |
|---|---|
| Number of episodes of the donor site infection. Timepoint: Before the intervention and 3, 6, 8 and 10 days after the intervention. Method of measurement: Inspection of the donor site and/or microbial culture of wound secretions.;Number of episodes of the donor site bleeding. Timepoint: Before the intervention and 3, 6, 8 and 10 days after the intervention. Method of measurement: Inspection of the donor site. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNaemeh Nikvarz
Kerman University of Medical Sciences
Outcome results
None listed