Efficacy and Tolerability of a Fractional Ablative Erbium Laser for Axillary Scarring for Hidrade⦠(NCT05470322) | Clinical Trial Compass
WithdrawnNot Applicable
Efficacy and Tolerability of a Fractional Ablative Erbium Laser for Axillary Scarring for Hidradenitis Suppurativa Patients
Stopped: No patients were able to consented/enrolled into the study during the period of time the study was approved by the IRB. Study officially withdrawn with the IRB on 11/24/2025.
United States0Started 2026-01
Plain-language summary
Single center, open-label, baseline-controlled study evaluating the use of a Sciton fractionated ablative laser in the treatment of Hidradenitis Suppurativa (HS) scarring.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Healthy males and females, ā„ 18 years of age at time of informed consent with no upper age limit, seeking treatment for HS scarring in the axillary region.
* Subjects must voluntarily sign and date an IRB approved informed consent form.
* Subjects with diagnosis of HS (Hidradenitis Suppurativa) scarring recorded over the past 6 months.
* Subject has an HS PGA (Hidradenitis Suppurativa Physician's Global Assessment) Scale of 0 or 1
* Able to read, understand and voluntarily provide written informed consent.
* Subjects are determined to be healthy, non-smokers.
* Subjects able and willing to comply with the treatment protocol and follow-up schedule and requirements.
* Understand and accept the obligation not to undergo any other procedures in the areas to be treated through the follow-up period.
Exclusion Criteria:
* Subject does not have the capacity to consent to the study.
* Subject underwent any medical-grade scar treatments (ie, lasers, excision procedures, topical prescriptions for scars) in the past 6 months prior to enrollment in the study.
* Any history of keloid scarring.
* Any previous surgical procedure in the treatment area in the past 12 months, or major surgery in the last 6 months.
* History of immunosuppression/immune deficiency disorders (including AIDS and HIV infection), and/or any history of systemic chemotherapy for prior 12 months.
* Subject has no health contraindications to receiving local lidocaine and epinephrine injections, iā¦