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Evaluation of effects of calcipotriol ointment on healing of skin graft donor site

Phase 3
Recruiting
Conditions
Burn injury.
Burn and corrosion, body region unspecified
Registration Number
IRCT20150609022637N5
Lead Sponsor
Kerman University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
48
Inclusion Criteria

Patients undergo split thickness skin graft
Patients sign informed consent form

Exclusion Criteria

Infection of the donor site
Bleeding of the donor site
Pregnancy
Lactation
Hypercalcemia
Hyperphosphatemia
Renal failure
Hepatic impairment
Sepsis

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
umber 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.
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