The effect of prp enriched with vitamin C on the skin donor site
Not Applicable
Recruiting
- Conditions
- Burn patients.
- Registration Number
- IRCT20220620055224N1
- Lead Sponsor
- Kerman University of Medical Sciences.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Burn patients need a graft
Exclusion Criteria
Addiction
Underlying disease
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessing pain using a pain scale. Timepoint: The amount of pain on a daily basis for up to 5 days. Method of measurement: Patient pain rate using Visual analog scale(VAS).;Examining the pathology of the donnor graft site. Timepoint: Pathology examination on the fifth day after graft removal. Method of measurement: microscope.
- Secondary Outcome Measures
Name Time Method Evaluation of patients' pain based on visual analog scale(VAS). Timepoint: Daily. Method of measurement: Visual analouge scale.