A prospective randomized control trial comparing the effect of Chloramphenicol ointment with Recombinant Human Epidermal Growth Factor on facial burn wound healing
Not Applicable
- Conditions
- Second degree burn wound Facial burn wound healingRecombinant Human Epidermal Growth Factor promote wound healingBurnFacial burnBurn wound healingChloramphenicol ointmentRecombinant Human Epidermal Growth FactorrhEGF
- Registration Number
- TCTR20171004003
- Lead Sponsor
- Faculty of Medicine Siriraj Hospital, Mahidol University, Thailand
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending (Not yet recruiting)
- Sex
- All
- Target Recruitment
- 36
Inclusion Criteria
- Age 18-65 years old
- Second degree facial burn wound area > 1 %BSA
- Burn in 48 hours
Exclusion Criteria
- Immunocompromised host
- Using steroids, chemotherapy, immunosuppressive drugs
- Allergy to chloramphenicol, recombinant human epidermal growth factor or Isopropyl p-Hydroxybenzoate
- Breast feeding or pregnancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Complete healing day Evaluate every 2 days Area of granulation tissue that measure from eKare inSightâ„¢ 3D Wound
- Secondary Outcome Measures
Name Time Method Effect of drug on wound pain Evaluate every 2 days after change wound dressing for 30 minutes Numeric pain score [0 to 10],Effect of drug on wound infection rate Evaluate every 2 days Fever, Wound appearance; erythema, swelling, pus discharge, fever, swab culture ; bacteria >10^5 CFU,Effect of drug on scar appearance 2,6 months after complete healing wound Vancouver scar scale,Side effects of drug Evaluate every 2 days after change wound dressing for 30 minutes Rash Irritation