Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
All Genders
ID07151599

Randomized Controlled Trial Comparing Fractional Erbium:Glass and Thulium Lasers Versus Microneedling for Atrophic Acne Scars

Led by University of Nove de Julho · Updated on 2025-11-26

84

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to compare two treatments for atrophic acne scars on the face in adults between 18 and 30 years old. It evaluates whether the combined use of fractional Erbium:Glass and Thulium lasers results in better scar improvement than microneedling. Acne scars can impact self-esteem and quality of life, so finding more effective treatments is important for patients. The trial is a randomized controlled study sponsored by the University of Nove de Julho. Participants receive one of two treatments assigned by chance: microneedling with an electronic pen using a 12-needle cartridge at 2mm depth, or a combination of fractional Erbium:Glass laser focused on scarred areas followed immediately by fractional Thulium laser applied over the full face. Both groups undergo three treatment sessions spaced four weeks apart. The lasers deliver energy to promote skin remodeling, while microneedling stimulates repair through small skin punctures. Throughout the study, participants are assessed before treatment, and then at 30 days and up to 16 weeks after the last session. Independent evaluators use standardized photos and an acne scar grading scale to measure improvement. Patients also report their satisfaction, pain levels, and any side effects during follow-up visits up to 90 days after treatment. Quality of life and aesthetic improvement are also evaluated to understand overall treatment effects.

CONDITIONS

Brief Title

Efficacy of Combined Fractional Er:Glass and Thulium Lasers Versus Microneedling for Atrophic Acne Scars

Who Can Participate

Age: 18Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Fitzpatrick skin phototypes I to VI
  • Presence of atrophic acne scars on the face
  • Aged between 18 and 45 years
Not Eligible

You will not qualify if you...

  • Decompensated systemic diseases
  • Any active infection (viral such as herpes, bacterial, or fungal)
  • Pregnant or breastfeeding women
  • Presence of hypertrophic or keloid scars
  • Current use of anticoagulant or antiplatelet medications
  • History of hemophilia or coagulation disorders
  • Current use of anti-inflammatory drugs or corticosteroids
  • Use of retinoids, including isotretinoin, within the past 6 months
  • Exposure to sunlight within the past 15 days
  • Undergoing or having undergone aesthetic facial or scar treatments within 180 days prior to study start
  • Presence of active acne (except occasional isolated lesions)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Approximately 12 weeks

Participants receive one of two treatments for atrophic acne scars: either microneedling or a combination of fractional Erbium:Glass and Thulium lasers. Each participant undergoes three treatment sessions spaced four weeks apart.

3 treatment sessions, each 4 weeks apart

Follow-up

Duration - Up to 90 days after the last session

Participants are monitored for up to 90 days after the last treatment session to assess scar improvement, patient satisfaction, and any adverse events.

Visits at 30 days and 90 days after the last treatment session

Trial Site Locations

Total: 1 location

1

Espaço Conceito Medical San

São Paulo, Brazil

Actively Recruiting

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Research Team

L

Luciana Khachikian, Master student

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Frequently Asked Questions

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