Comparing the healing effect of dried and acellular human amniotic membrane with Mepitel as coverage of skin graft donor areas
Phase 2
- Conditions
- Skin wound.Open wound of unspecified body region
- Registration Number
- IRCT201511118177N12
- Lead Sponsor
- Royan Institute for Stem Cell Biology and Technology (RI-SCBT)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
age 16-60 years, requiring skin grafting, informed consent form completion
Exclusion criteria: having underlying disease
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Wound healing. Timepoint: observation, examination and photography on days 4, 8 and 12 after surgery. Method of measurement: observation, examination and photography.
- Secondary Outcome Measures
Name Time Method Pain. Timepoint: Days four, eight and twelve after surgery. Method of measurement: Visual analog scale.;Infection. Timepoint: Days four, eight and twelve after surgery. Method of measurement: Observation and examination.;Scar. Timepoint: Three and six months after surgery. Method of measurement: Vancouver scale.