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1470nm Laser for the Treatment of Androgenetic Alopecia and Scarring Alopecia

Montefiore Medical Center · with Sciton · NCT05460611

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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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1470nm Laser for the Treatment of Androgenetic Alopecia and… (NCT05460611) | Bored Studies