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Clinical Trials/NCT06566300
NCT06566300RecruitingNot Applicable

Autologous Nanofat Grafting by Injection Versus With Microneedling in Post-burn and Traumatic Atrophic Scars

Alexandria University1 site in 1 country30 target enrollmentStarted: November 1, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
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

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dalia Ibrahim Halwag

Principal investigator

Alexandria University

Study Sites (1)

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