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

Last updated: November 2, 2024
Sponsor: Alexandria University
Overall Status: Active - Recruiting

Phase

N/A

Condition

Skin Wounds

Treatment

injection of autologous nanofat grafting

microneedling with autologus nanofat graft

Clinical Study ID

NCT06566300
Nanofat scar
  • Ages 18-60
  • All Genders

Study 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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Males and females between 18-60 years old. 2. Post-burn or traumatic atrophicscar > 6 months duration (16). 3. Patients not receiving any treatments for thescar within the past 3 months.

Exclusion

Exclusion Criteria:

  1. Patients with contractures, hypertrophic and keloid scars. 2. Patients withhistory of bleeding disorders or coagulopathy, or on anticoagulant therpy.

  2. Diabetes and other systemic diseases that may be complicated by the procedure.

  3. Pregnant and lactating females. 5. BMI less than 18.5 6. Patients with scars atthe donor site

Study Design

Total Participants: 30
Treatment Group(s): 2
Primary Treatment: injection of autologous nanofat grafting
Phase:
Study Start date:
November 01, 2024
Estimated Completion Date:
February 28, 2025

Connect with a study center

  • Alexandria University

    Alexandria,
    Egypt

    Active - Recruiting

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