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The effect of atheromatous wound dressing on the improvement of the skin graft site

Phase 1
Recruiting
Conditions
Burns.
Burns and corrosions of multiple body regions
Registration Number
IRCT20130819014404N4
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
10
Inclusion Criteria

Adult patients between 18-55 years old
Burnt injury less than 10% of total body surface area
Needing autograft
Informed consent for participation in the study

Exclusion Criteria

Electrical burn
Chemical burn
Diabetes
Chronic liver failure
Chronic kidney failure
Advanced heart disease
Severe malnutrition with albumin less than 2.5 grams per deciliter
Use of immunosuppressive drugs
Advanced metastatic cancers
Use of immunosuppressive drugs
Connective tissue diseases

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain score. Timepoint: Resting on the first and second day and on the third day before and at the time of changing the dressing and on the seventh day. Method of measurement: Visual analogue scale.;Length of hospital stay. Timepoint: At discharge time. Method of measurement: Day.;Donor site wound healing time. Timepoint: Day 3 and 7. Method of measurement: Imaging and clinical judgment.
Secondary Outcome Measures
NameTimeMethod
Symptoms of allergies. Timepoint: Day 3 and 7. Method of measurement: Clinical examination.
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