Efficacy and Tolerability of a Fractional Ablative Erbium Laser for Axillary Scarring for Hidradenitis Suppurativa Patients

NCT ID: NCT05470322

Last Updated: 2025-12-17

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2026-01-31
• Study Completion Date: 2027-07-31

Brief 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.

Detailed Description

Single center, open-label, baseline-controlled study evaluating the use of a Sciton fractionated ablative laser in the treatment of Hidradenitis Suppurativa (HS) scarring. The device is FDA approved for the treatment of scarring in all skin types. The study team seeks to observe the efficacy and tolerability in patients without active HS lesions. The study may enroll up to 19 subjects looking for improvement in their HS scarring in the axillary region. The subjects will receive treatment with the Sciton Joule Er:YAG 2940nm laser along with treatment with topical tretinoin, hydroquinone, and hydrocortisone starting 1 month prior to first laser treatment as per standard of care for scar treatment. Each patient will receive 3 treatments spaced approximately one month apart. The patients will be surveyed about their quality of life due to HS scarring, as well as their perspectives on their axillary scarring before and after their assigned treatments. All patients included in the study will have no contraindications to either laser or the use of standard treatment protocol (tretinoin and hydroquinone). Subjects in the laser group will complete a DLQI (Dermatology Life Quality Index) survey, patient satisfaction survey, and clinical photographs at each treatment visit and at follow-up 1, 2, and 3 months after the last treatment. Subjects in the topical treatment group will be evaluated at the initial visit, month 3 and month 6.

Conditions

Hidradenitis Suppurativa; Scarring

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Laser Treatment

The parameters of the laser will be set according to optimal operation protocol and in accordance with guidelines set forth by Sciton. Each laser treatment will take approximately 10 to 15 minutes per subject to target HS scarring.

Group Type: EXPERIMENTAL

Er: YAG laser

Intervention Type: DEVICE

Patients will be treated with laser for their HS scarring.

Interventions

Er: YAG laser

Patients will be treated with laser for their HS scarring.

Intervention Type: DEVICE

Other Intervention Names

laser; fractional ablative laser

Eligibility Criteria

Inclusion Criteria

• Healthy males and females, ≥ 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, including but not limited to any form of heart disease or arrhythmia, untreated or uncontrolled severe hypertension, uncontrolled hyperthyroidism, uncontrolled diabetes, pheochromocytoma, Cocaine use.
• History or current use of the following prescription medications:Accutane or other systemic retinoids within the past twelve months, Tricyclic antidepressant, monoamine oxidase inhibitors, B-blocker
• Smoking or vaping in the past 12 months.
• History of an allergy or an adverse reaction to hydroquinone or tretinoin.
• History of photosensitivity and/or connective tissue disease.
• History of uncontrolled diabetes, hypertension and depression.
• History of ongoing pregnancy, active breastfeeding, cancer, and epilepsy.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Montefiore Medical Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Kseniya Kobets, MD

Role: PRINCIPAL_INVESTIGATOR

Albert Einstein College of Medicine Montefiore Medical Center

Locations

Montefiore Einstein Advanced Care

Elmsford, New York, United States

Countries

United States

Other Identifiers

2022-14262

Identifier Type: -

Identifier Source: org_study_id