Safety and Efficacy of 1550nm Fractional Laser Treatment for Acne Scars in Fitzpatrick Type IV-VI Skin

Henry Ford Health System15 enrolled

Overview

Fractionated laser resurfacing is commonly used as a treatment for acne scarring in fair skinned individuals. This study aims to test the efficacy and safety in darker skin types. Patients are randomized to either the 10mJ 40mJ dosages and receive a total of five treatments at 17% one month apart. Improvement is judged by a dermatologist as 0-25%, 25-50%, 50-75% or 75-100%. Side effects such as pigmentary abnormalities and pain are also evaluated.

Background: Ablative resurfacing lasers are effective for treatment of acne scars, but they have a high risk of complications. Fractional lasers have less severe side effects but more moderate efficacy than ablative devices. Studies were performed in individuals with Fitzpatrick skin type I to VI. Objective: To determine the efficacy and safety of an erbium 1,550-nm fractional laser in the treatment of facial acne scars in Fitzpatrick skin types IV to VI. Methods: We conducted a prospective, single-blind, randomized trial in patients with acne scars (n=15), skin type IV to VI, with a 1,550-nm erbium fractionated laser. Patients were divided into two groups; one was treated with 10 mJ and the other with 40 mJ. Five monthly laser sessions were performed. A patient questionnaire was distributed.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Acne Scarring

Interventions

Fractionated Laser ResurfacingPROCEDURE

Eligibility

Sex: ALLMin age: 18 YearsMax age: 59 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Male or female voluntary patients between the ages of 18 and 59 with Fitzpatrick skin type IV-VI as verified by one of the investigators * Patients with clinical diagnosis of ice pick, rolling, or boxcar type ane scarring * Patients able to follow instructions * If patient has a history of cold sores (herpes labialis) they must be willing to take prophylactic valtrex * Written informed consent from the patients (Appendix II) Exclusion Criteria: * Children (less than 18 years old) * Pregnant or lactating women * Personal history of keloids or hypertrophic scarring * Active acne requiring topical or oral therapy * Accutane or other oral retinoid in past year * Patients with a known allergy to lidocaine * Allergy to valacyclovir in a patient that needs prophylaxis * Patients with an unstable or non controlled underlying medical problem * Patients who are not able to follow instructions * Patients who have participated in a study within the 3 months prior to study entry * Patients who refuse to give written informed consent * Patients with a history of a pigmentary abnormality

Locations (1)

Henry Ford Health System

Detroit, Michigan, United States

Outcomes

Primary Outcomes

Improvement in acne scarring.

Blinded evaluators will score improvement of acne via photographs using a quartile grading scale (0 = no improvement, 1 = minor improvement \[1-25%\], 2 =moderate improvement \[26-50%\], 3 =marked improvement \[51-75%\], 4 = very significant improvement \[76-100%\]).

Time frame: 6 months

Secondary Outcomes

Dyspigmentation

dyspigmentation will be assessed separately from acne scarring via photographs with blinded evaluators on a scale of 1- 3. 1 (minimal amount of hyperpigmentation), 2 (moderate hyperpigmentation) and 3 (severe amount of hyperpigmentation) depending on the degree of hyperpigmentation compared with their baseline photo.

Time frame: 6 months

Pain with treatment

subjects will report any pain with treatment on a 0-10 scale, with zero indicating no pain and 10 indicating the worst pain

Time frame: 5 months

Data from ClinicalTrials.gov

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