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This study aims to evaluate the efficiency autologous nanofat injection versus autologous nanofat delivered by microneedling in management of post burn atrophic and traumatic scars.
Enrollment
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Inclusion criteria
Exclusion criteria
Patients with contractures, hypertrophic and keloid scars. 2. Patients with history of bleeding disorders or coagulopathy, or on anticoagulant therpy.
Diabetes and other systemic diseases that may be complicated by the procedure.
Pregnant and lactating females. 5. BMI less than 18.5 6. Patients with scars at the donor site
Primary purpose
Allocation
Interventional model
Masking
30 participants in 2 patient groups
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Central trial contact
Dalia I Halwag, PhD, MD
Data sourced from clinicaltrials.gov
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