NCT06566300RecruitingNot Applicable
Autologous Nanofat Grafting by Injection Versus With Microneedling in Post-burn and Traumatic Atrophic Scars
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Alexandria University
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- change in the scar by by the patient and observer scar assessment scale (POSAS).
Study Overview
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.
Study Design
- Study Type
- Interventional
- Allocation
- Non Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 60 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Males and females between 18-60 years old.
- •Post-burn or traumatic atrophic scar > 6 months duration (16).
- •Patients not receiving any treatments for the scar within the past 3 months.
Exclusion Criteria
- •Patients with contractures, hypertrophic and keloid scars.
- •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.
- •BMI less than 18.5
- •Patients with scars at the donor site
Outcomes
Primary Outcomes
change in the scar by by the patient and observer scar assessment scale (POSAS).
Time Frame: 6 months after the proceedure
patient and observer scar assessment scale score will be uesd
Secondary Outcomes
No secondary outcomes reported
Investigators
Dalia Ibrahim Halwag
Principal investigator
Alexandria University
Study Sites (1)
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