1470nm Laser for the Treatment of Androgenetic Alopecia and Scarring Alopecia
Montefiore Medical Center · with Sciton · NCT05460611
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–99 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 10
- US sites recruiting
- 1
- Study start
- December 7, 2023
- Record last updated
- October 1, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
Single-center, open-label, baseline-controlled, pilot study evaluating the use of a Nonablative 1470 nm laser for the treatment of androgenetic alopecia and scarring alopecia.
Being studied: Sciton HALO 1470nm Non-ablative laser
Conditions: Scarring Alopecia; Androgenetic Alopecia
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Healthy males and females, ≥ 18 years of age at time of informed consent, seeking treatment for hair loss
- Subject must voluntarily sign and date an IRB approved informed consent form
- Subjects with diagnosis of biopsy proven androgenetic alopecia or scarring alopecia with hair loss recorded over the past 6 months
- Subjects must have a stable hair loss treatment regimen with a plateau in results for at least 3 months
- Able to read, understand and voluntarily provide written informed consent
- Subject is determined to be healthy, non-smoker who agrees not to make any changes to their daily hair treatment regimen during the study
- Subjects able and willing to comply with the treatment protocol and follow-up schedule and requirements
- Understands and accepts 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 has other types of alopecia of the scalp like alopecia areata
- History of intralesional steroid injections to the scalp in the last 12 months
- Pregnant women
- Any medical condition that in the consideration of the investigator, would present an increased risk of a photosensitivity reaction to the subject
- Any previous surgical procedure in the treatment area in the past 12 months, or major surgery in the last 6 months
- Allergy or history of prior reaction to lidocaine
- History of immunosuppression/immune deficiency disorders (including AIDS and HIV infection), and/or any history of systemic chemotherapy for prior 12 months
- History or current use of the following prescription medications:
i. Immunosuppressive medications/biologics, 6 months prior to and during the study ii. Accutane or other systemic retinoids within the past twelve months
- Smoking or vaping in the past 12 months
- History of uncontrolled hyperlipidemia, diabetes mellitus, hepatitis, or bleeding disorders
- History of major depressive disorders or endocrine disorders including but not limited to; hypothyroidism, Hashimoto's thyroiditis, or hyperthyroidism
Recruiting US locations
Montefiore Einstein Advanced Care
Elmsford, NY 10523
Site contact: Gabriela Gjini · 914-457-4130 · ggjini@montefiore.org
Study contacts (from the official record)
- Ryan Chan, BA · 631-553-2203 · ryachan@montefiore.org
- Kseniya Kobets
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