Recruiting NCT06566300
Autologous Nanofat Grafting by Injection Versus With Microneedling in Post-burn and Traumatic Atrophic Scars
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: injection of autologous nanofat grafting, microneedling with autologus nanofat graft.
- Who it may be relevant to
- Registry conditions: Scars. Basic parameters: 18 years — 60 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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.
Interventions
- Procedure injection of autologous nanofat grafting
Injection of nanfat graft - Procedure microneedling with autologus nanofat graft
delivery of nanofat graft with microneedling
Primary outcome measures
- change in the scar by by the patient and observer scar assessment scale (POSAS). [Time frame: 6 months after the proceedure]
Eligibility criteria
Inclusion criteria
- 1\. 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.
Exclusion criteria
- 1\. Patients with contractures, hypertrophic and keloid scars. 2. Patients with history of bleeding disorders or coagulopathy, or on anticoagulant therpy.
3\. Diabetes and other systemic diseases that may be complicated by the procedure.
4\. Pregnant and lactating females. 5. BMI less than 18.5 6. Patients with scars at the donor site
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Non-randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Egypt · 1 center
- Alexandria University — Alexandria
Identifiers
NCT: NCT06566300 · Nanofat scar