Is NCT06885112 recruiting in New York, NY?

Yes, NCT06885112 is currently recruiting participants at its New York, NY location. This hair loss clinical trial is actively enrolling qualified participants.

How do I join the hair loss clinical trial in New York?

To join this clinical trial in New York, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

Is participation in this New York clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

Hair Loss Clinical Trial in New York, NY

Who Can Participate

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.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in New York?

Yes, this clinical trial (NCT06885112) has an active research site in New York, NY that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Hair Loss Treatment Options in New York, NY

If you're searching for hair loss treatment options in New York, NY, this clinical trial (NCT06885112) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our New York research site is actively enrolling participants for this clinical trial. You'll receive care from experienced hair loss specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all hair loss clinical trials near you to find additional studies recruiting in your area.

Hair Loss Clinical Trial in New York, NY

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About This Hair Loss Study in New York