Efficacy and Safety of a 1064-nm Nd:YAG Picosecond Laser Versus a 1927-nm Fractional Laser for Atrophic Acne Scars.

NCT ID: NCT07153679

Last Updated: 2025-09-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

38 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-01-01

Study Completion Date

2021-08-01

Brief Summary

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Atrophic acne scars are common disfiguring skin problems, especially in the Asian population prone to Post-inflammatory Hyperpigmentation (PIH), and their treatment is highly challenging. 1064 nm microlens array picosecond laser (P-MLA) based on optomechanical effect and 1927 nm segmented thulium laser (FTL) based on photothermal effect are two emerging therapeutic techniques, but there is a lack of strict clinical evidence for direct comparison in the Asian population. This study aims to directly compare the clinical efficacy, safety and tolerability of 1064 nm P-MLA and 1927 nm FTL in the treatment of atrophic acne scars in the Asian population through a randomized, half-face controlled, evaluator blind trial.

Detailed Description

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Conditions

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Acne Scar Acne Scars - Atrophic

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Caregivers Outcome Assessors

Study Groups

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1064-nm Nd:YAG Picosecond Laser Group

1064-nm Nd:YAG Picosecond Laser Device (Picocare 450, WONTECH, Daejeon, South Korea)

Group Type EXPERIMENTAL

1064-nm Nd:YAG Picosecond Laser

Intervention Type DEVICE

Treatment was performed using 1064 nm Nd:YAG microlens array picosecond laser (Picocare 450, WONTECH, Daejeon, South Korea). Received three treatments, with a 4-week interval between each treatment.

1927-nm Fractional Thulium Laser Group

1927-nm Fractional Thulium Laser Device (Lavieen, WONTECH, Daejeon, South Korea)

Group Type EXPERIMENTAL

1927-nm Fractional Thulium Laser

Intervention Type DEVICE

Treatment was performed using 1927-nm thulium fractional laser (Lavieen, WONTECH, Daejeon, South Korea). Received three treatments, with a 4-week interval between each treatment.

Interventions

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1064-nm Nd:YAG Picosecond Laser

Treatment was performed using 1064 nm Nd:YAG microlens array picosecond laser (Picocare 450, WONTECH, Daejeon, South Korea). Received three treatments, with a 4-week interval between each treatment.

Intervention Type DEVICE

1927-nm Fractional Thulium Laser

Treatment was performed using 1927-nm thulium fractional laser (Lavieen, WONTECH, Daejeon, South Korea). Received three treatments, with a 4-week interval between each treatment.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Aged between 18 and 40.
* Symmetrical atrophic acne scars on both sides of the face.

Exclusion Criteria

* Uncontrolled active acne.
* Pregnant and lactating women.
* Infectious skin diseases at the treatment site.
* Have taken retinoid drugs orally within the past 6 months.
* Photosensitive individuals or those who have used photosensitive drugs within 2 weeks.
* Keloid constitution.
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Second Affiliated Hospital of Xi'an Jiaotong University

OTHER

Sponsor Role lead

Responsible Party

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Weihui Zeng

professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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The second affiliated hospital of Xi'an Jiaotong University

Xi’an, Shanxi, China

Site Status

Countries

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China

Other Identifiers

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2021013

Identifier Type: -

Identifier Source: org_study_id

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