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

ConditionScars

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age18-60

SponsorAlexandria University

About this trial

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

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

injection of autologous nanofat grafting
Procedure/Surgery
Injection of nanfat graft
microneedling with autologus nanofat graft
Procedure/Surgery
delivery of nanofat graft with microneedling

Treatment groups

30 Participants

are divided into 2 treatment groups

Group A: injection of autologous nanofat graftingExperimental treatment 1 intervention

Group B: microneedling with autologous nanofat graftExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

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

patient and observer scar assessment scale score will be uesd

Time frame

6 months after the proceedure

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Alexandria University

Lead sponsor

Source ClinicalTrials.gov

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