Which laser erases acne scars better? a Head-to-Head test
NCT ID NCT03850925
First seen Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time
Summary
This study compares two laser treatments for facial acne scars: a picosecond Nd:YAG laser with a special lens and a nonablative fractional laser. Participants receive four sessions of one laser type, and researchers measure changes in scar severity using a standard grading scale. The goal is to see which laser is more effective at improving the appearance of acne scars.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Laser therapy (picosecond Nd:YAG laser with diffractive lens array vs. nonablative fractional laser)
- What this could lead to
- If successful, this could identify a more effective laser treatment for reducing the appearance of acne scars.
- What could go wrong
- The trial is small (25 participants) and early-stage, so results may not apply broadly. Laser treatments can cause temporary redness, swelling, or pigmentation changes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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25 people
The number who actually took part.
- Started
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May 2019
- Finished
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Apr 2020
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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19 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Subjects with facial atrophic acne scars * Subjects who observe the schedules and protocols of the clinical trial * Subjects who give informed consent to participate in the clinical trial Exclusion Criteria: * Subjects who have active acne under treatment * Subjects who had received any other treatments for acne scarring for 6 months prior to the first treatment * Subjects who underwent other treatments including chemical, mechanical or laser resurfacing during the study period * Subjects who have current acute illness * Subjects who are considered inappropriate for the clinical trial under the judgement of investigators
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Dongtan Sacred Heart Hospital, Hallym Universtiy College of Medicine
Hwaseong-si, Gyeonggi-do, 18450, South Korea
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