Laser zaps acne? small trial fizzles out
NCT ID NCT04466527
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a fractional carbon dioxide laser can improve moderate to severe acne in adults aged 18 to 40. Participants received up to 3 laser treatments and were followed for changes in blemish count and skin severity. The trial was terminated early and only enrolled 4 people, so results are very limited.
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
-
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
-
4 people
The number who actually took part.
- Started
-
Nov 2020
- Finished
-
Jul 2022
- Lead sponsor
-
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
-
18 to 40 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: 1. Subject must be able and willing to provide written informed consent and comply with the requirements of the study protocol; 2. In good general health, based on answers provided during the screening visit; 3. Subject must be able to read and understand English; 4. Any gender and any Fitzpatrick skin type; 5. Ages 18 through 40; 6. Subjects must have moderate to severe nodular active facial acne vulgaris (PGA 3 or 4) 7. Willing to sun protect treated area for the duration of enrollment in the study and 1 year after treatment; 8. Subjects must be ineligible for or have declined standard of care treatments (e.g. oral isotretinoin therapy). Exclusion Criteria: 1. Participation in another investigational drug or device clinical trial in the past 30 days; 2. Currently undergoing or wish to begin or continue topical treatments; 3. Are pregnant or lactating; 4. History of allergic reaction to topical anesthesia; 5. Subjects may not have undergone oral isotretinoin therapy within the past 12 months; 6. Currently take oral antibiotic or oral therapy for acne; 7. History of keloidal or hypertrophic scarring; 8. Laser treatment in past six months; 9. History of poor wound healing; 10. Clinically significant abnormal findings or conditions which might, in the opinion of the Investigator, interfere with study evaluations or pose a risk to subject safety during the study.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Acne vulgaris are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
MGH Clinical Unit for Research Trials & Outcomes in Skin
Boston, Massachusetts, 02114, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Acne may signal hidden hormonal disorder in young women
- Hormone tests may reveal who benefits most from acne drug
- Blood pressure drug takes on antibiotics for Women's acne
- Can radiofrequency waves outperform acne gels?
- Can adding a chemical peel to microneedling erase acne scars better?
- Can a beam of light boost acne treatment?