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

Description

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.

Conditions

Scarring Alopecia, Androgenetic Alopecia

Study Overview

Study Details

Study overview

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.

A Pilot Study Evaluating the Safety and Efficacy of a 1470nm Laser for the Treatment of Androgenetic Alopecia and Scarring Alopecia

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

Condition
Scarring Alopecia
Intervention / Treatment

-

Contacts and Locations

Elmsford

Montefiore Einstein Advanced Care, Elmsford, New York, United States, 10523

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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
  • * 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 regime 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.
  • * Subject does not have the capacity to consent to the study
  • * Subject has other types of alopecia of the scalp like alopecia areata
  • * Use of minoxidil or 5-alpha reductase inhibitors (i.e., finasteride, dutasteride) 3 months prior to screening date.
  • * History of intralesional steroid injections to the scalp in the last 12 months
  • * 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:
  • * Smoking or vaping in the past 12 months.
  • * History of 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.

Ages Eligible for Study

18 Years to 99 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Montefiore Medical Center,

Kseniya Kobets, MD, PRINCIPAL_INVESTIGATOR, Albert Einstein College of Medicine Montefiore Medical Center

Study Record Dates

2025-12