Burn. Calcification and ossification of muscles associated with burns, unspecified site
Conditions
Interventions
Intervention 1: Intervention group: donor site in this group was covered with amniotic membranes made by Royan Cells Co 10 x 15 cm, Vaseline gauze, and wet dressing. Intervention 2: Control group: The
Sponsors
Sabzevar University of Medical Sciences
Eligibility
Sex/Gender
All
Age
2 Years to 60 Years
Inclusion criteria
Inclusion criteria: Patients aged 2-60 years Grade 2 and 3 burn patients require autologous skin graft (STSG) and surgery
Exclusion criteria
Exclusion criteria: Connective tissue diseases, diabetes, malnutrition, septicemia, heart disease, kidney failure, cancer, chemotherapy and the use of corticosteroid drugs. Dissatisfaction patients to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Determination of pigmentation. Timepoint: Measurement of pigmentation on days 10, 20 and 30 after the intervention. Method of measurement: Photographic Morphometry.;Determination of epithelization. Timepoint: Measurement of epithelization on days 10, 20 and 30 after the intervention. Method of measurement: Photographic Morphometry.;Determination of superficial vascularity. Timepoint: Measurement of superficial vascularity on days 10, 20 and 30 after the intervention. Method of measurement: Photographic Morphometry.;Determination of granulation. Timepoint: Measurement of granulation on days 10, 20 and 30 after the intervention. Method of measurement: Photographic Morphometry. | — |
Secondary
| Measure | Time frame |
|---|---|
| Determine the amount of pain. Timepoint: Measurement of pain on days 10, 20 and 30 after the intervention. Method of measurement: Visual Analogue Scale of Pain Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Sahebkar
Sabzevar University of Medical Sciences
Outcome results
None listed