Acute deep burns and scar contracture.
Conditions
Interventions
Intervention 1: Intervention group: This intervention includes patients with deep second-degree burn wounds and burn scar contracture who receive a prepared absorbable dermal substitute with an area o
Sponsors
Iran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Age between 18 and 70 years Both genders Acute wound and scar contracture No history of wound or burn at the current site No acute mental illness No use of immunosuppressive drugs No massive unstable trauma Completed informed consent form
Exclusion criteria
Exclusion criteria: Pregnancy or breastfeeding Wounds on joints, face, perineum Patients with diabetic and infected wounds Presence of a chronic skin disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Take rate. Timepoint: End of study. Method of measurement: The “take rate” is estimated by observation by the plastic surgeon assigned to this study. Image J® software is used to calculate the graft percentage. This is done by measuring the area of ??the taken area relative to the original area.;Scar quality. Timepoint: End of study. Method of measurement: Vancouver scar scale.;Vascular supply. Timepoint: End of study. Method of measurement: Evaluation by laser Doppler device. | — |
Secondary
| Measure | Time frame |
|---|---|
| Healing time. Timepoint: End of the study. Method of measurement: Since the patient is under the supervision of a plastic surgeon during the treatment period, the wound healing time will be reported by the plastic surgeon, and the performance of the collagen dermal substitute will be evaluated and reviewed accordingly. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohamad Pezeshki Modaress
Iran University of Medical Sciences
Outcome results
None listed