Autologous Nanofat Grafting by Injection Versus With Microneedling in Post-burn and Traumatic Atrophic Scars
- Conditions
- Scars
- Interventions
- Procedure: injection of autologous nanofat graftingProcedure: microneedling with autologus nanofat graft
- Registration Number
- NCT06566300
- Lead Sponsor
- Alexandria University
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 30
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- Males and females between 18-60 years old. 2. Post-burn or traumatic atrophic scar > 6 months duration (16). 3. Patients not receiving any treatments for the scar within the past 3 months.
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Patients with contractures, hypertrophic and keloid scars. 2. Patients with history of bleeding disorders or coagulopathy, or on anticoagulant therpy.
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Diabetes and other systemic diseases that may be complicated by the procedure.
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Pregnant and lactating females. 5. BMI less than 18.5 6. Patients with scars at the donor site
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description injection of autologous nanofat grafting injection of autologous nanofat grafting Two separate scars with similar properties or splitting of one large post-burn atrophic scar. One (part of the) scar will be treated by injection of autologous nanofat grafting and the other (part of the) scar will be treated by microneedling with autologous nanofat graft. microneedling with autologous nanofat graft microneedling with autologus nanofat graft Two separate scars with similar properties or splitting of one large post-burn atrophic scar. One (part of the) scar will be treated by injection of autologous nanofat grafting and the other (part of the) scar will be treated by microneedling with autologous nanofat graft.
- Primary Outcome Measures
Name Time Method change in the scar by by the patient and observer scar assessment scale (POSAS). 6 months after the proceedure patient and observer scar assessment scale score will be uesd
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Alexandria University
🇪🇬Alexandria, Egypt