Comparison of pressure dressing and stapler in skin graft
Not Applicable
- Conditions
- Burn.
- Registration Number
- IRCT20100628004256N9
- Lead Sponsor
- Ardabil University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Patients with 2nd and 3rd degree burns
Patients in the age range of 30-60 years
Not taking immunosuppressive drugs
No underlying diseases (diabetes, chronic Renal failure, etc.)
No addiction and heavy smoking
obtaining informed consent
Exclusion Criteria
A burn with an extent of more than 50% that it is not possible to remove the healthy skin as a scar
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Skin graft in terms of necrosis. Timepoint: ?During surgery, 5 and 7 days after graft. Method of measurement: The grafts of two areas will be studied in terms of necrosis, and finally the quality of scars (based on the examination and judgment of the surgeon) in the two areas of the burn.;Skin graft in terms of infection. Timepoint: ?During surgery, 5 and 7 days after graft. Method of measurement: The grafts of two areas will be studied in terms of infection, and finally the quality of scars (based on the examination and judgment of the surgeon) in the two areas of the burn.;Skin graft in terms of necrosis. Timepoint: ?During surgery, 5 and 7 days after graft. Method of measurement: The grafts of two areas will be studied in terms of displacement and finally the quality of the grips (based on the examination and judgment of the surgeon) in the two regions of the burn.
- Secondary Outcome Measures
Name Time Method