Recruiting

Fractional LaserClinical Study to Evaluate the Improvement in Hair Loss in Skin of Color Treated With Fractional Non-Ablative Laser

Sponsor:

Lumenis Be Ltd.

Code:

NCT06885112

Conditions

Hair Loss

Eligibility Criteria

Sex: All

Age: 21 - 55

Healthy Volunteers: Accepted

Interventions

FoLix treatment for improving the scalp hair appearance

Study Details

Brief summary:

The study incudes 18 to 55 y/o healthy subjects with moderate hair loss stage and Fitzpatrick skin type 5 or 6

Conditions

Hair Loss

Study ID

NCT06885112

Start date

Feb 21, 2025

Status verified date

Mar, 2025

Completion date

Feb 21, 2027

Anticipated

Primary completion date

Feb 21, 2027

Anticipated

Eligibility Criteria

Sex: All

Age: 21 - 55

Healthy Volunteers: Accepted

Inclusion Criteria:

Male and females between 21 - 55 years of age, inclusive.
Have Fitzpatrick Skin Type V to VI.
Have mild to moderate hair loss (Ludwig scale I-II for women, Norwood-Hamilton scale I-III for males)
Have self-reported thinning or hair loss for more than 6 months prior to screening but less than 5 years.
Clinically confirmed to have hair loss or thinning by the investigator via physical exam
Didn't receive hair-loss treatments or participated in a clinical study using 1565 NAFL device
In good general health, as determined by the Investigator
Willing and able to attend all study visits
Willing to maintain the same hair style as at the Screening Visit for the duration of the study. If coloring hair, willing to color it with the same frequency of usage as in the past, making sure not to color within 1-week before and 1-week after an in-office appointment
Willing to use a mild non-medicated shampoo and conditioner for the duration of the study (medicated shampoo and conditioner refer to any prescription shampoo or conditioner as well as any over-the counter medicated shampoo or conditioner, such as those for treatment of dandruff or promoting hair growth)
Have a negative urine pregnancy test at screening and be using, and continue to use for the duration of the study, an effective contraception method (i.e., abstinence, barrier control, intrauterine device \[IUD\], or hormonal \[estrogen/progestin\] contraceptives) for at least one menstrual cycle prior to study; if using IUD or hormonal contraceptives - then at least 2 years prior to screening, the initiation of which should not have been associated with initiation of hair loss/thinning.
Be willing and able to cooperate with the requirements of the study including images taken using a smart camera (multi-spectral) of several skin conditions
Voluntarily sign and date an informed consent agreement approved by the Institutional Review Board
Be able to complete and understand the various rating instruments in English
Sponsor approved global image assessment of degree of thinning / hair loss

Exclusion Criteria:

Clinical diagnosis of alopecia areata or scarring forms of alopecia
Patient is of skin type I-IV
Scalp hair loss on the treatment area, due to disease, injury, or medical therapy
Subjects who are pregnant, planning to become pregnant or breastfeeding. A urine pregnancy test will be done to rule out pregnancy. Subjects of childbearing potential who are not using an approved method of birth control (oral contraceptives, IUD, contraceptive implant, barrier methods with spermicide or abstinence). Females of non-childbearing potential are defined as postmenopausal (e.g.: absence of menstrual bleeding for one year), hysterectomy or bilateral oophorectomy
Current skin disease (e.g., psoriasis, atopic dermatitis, skin cancer, eczema, sun damage, seborrheic dermatitis), cuts and or abrasions on the scalp or condition (e.g., sunburn, tattoos) on the treatment area that, in the opinion of the Investigator, might put the subject at risk or interfere with the study conduct or evaluations
Participated in a previous 1565 NAFL study or treatment
History of surgical correction of hair loss on the scalp/ Hair transplants.
Use of any products or devices purported to promote scalp hair growth (e.g., finasteride or minoxidil) within the 90 days prior to the Baseline Visit.
Use of anti-androgenic therapies (e.g., spironolactone, flutamide, cyproterone acetate, cimetidine) within 60 days prior to the Baseline Visit.
No history of burning, flaking, itching, and stinging of the scalp.
A chronic condition of high severity dandruff.
History of malignancy (except scc and bcc skin cancers) or undergoing chemotherapy or radiation treatments.
A known history of autoimmune thyroid disease, any other thyroid disorder/abnormality or other autoimmune disorders that in the opinion of the investigator may interfere with the study treatment.
A known history of untreated or uncontrolled depression or bipolar disease or any other condition that may impact the subject's participation.
Recent utilization of low level lasers for treating hair loss (past 6 months).
Has any condition that the treating investigator or PI thinks may put the Subject at risk or interfere with their participation in the study.
Is involved in any injury litigation claims.
Known history or recent bloodwork indicating iron deficiency (ferritin level is less than 30 ng/mL), bleeding disorders or platelet dysfunction syndrome as well as subjects receiving anticoagulant therapy or smokers with usage >20 cigarettes/day.
Use of any medications that are known to potentially cause hair loss or affect hair growth, as determined by PI.

Study Design

Enrollment

40 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: healthy subjects with moderate hair loss stage and skin color type 5 or 6

The FoLix is FDA cleared for hair loss treatments in patients with skin type 1 to 4. It is no being studied for patients with skin type 5 and 6 to allow expending the product labeling

Interventions

FoLix treatment for improving the scalp hair appearance

The study patients will receive 4 FoLix treatment in 4 weeks intervals. the scalp hair improvement will be evaluated by 3 blinded assessors who shall review before and after images, as well as hair count data

Primary outcome measure

improvement in scalp hair appearance by comparing before and after images [ Time Frame: 12 months ]

Central Contacts and Locations

Central contacts

Keren Hayut

+972506905252 keren.hayut@lumenis.com

Locations

UnionDerm

Recruiting

New York, New York, United States, 10003

Contacts

Anne Chapas, MD, Medical Doctor

212-366-5400 research@unionderm.com

Principal Investigator:

Anne Chapas, MD, Medical Doctor

More Information

Sponsor

Lumenis Be Ltd.

Last update posted

Jan 2, 2026

Last verified

Mar, 2025

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-26. This information was provided to ClinicalTrials.gov by Lumenis Be Ltd. on 2026-01-02. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.