RecruitingNot Applicable

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

Egypt30 participantsStarted 2024-11-01

Plain-language 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.

Who can participate

Age range18 Years – 60 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

change in the scar by by the patient and observer scar assessment scale (POSAS).

Timeframe: 6 months after the proceedure

Trial details

NCT IDNCT06566300

SponsorAlexandria University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-02

Contact for this trial

Dalia I Halwag, PhD, MD

0201224489473 daliahalwag@gmail.com

View on ClinicalTrials.gov More Scars trials