Actively Recruiting

Phase Not Applicable
Age: 25Years +
All Genders
Healthy Volunteers
NCT05365360

Sham LaserCap vs. LaserCap SD vs. LaserCap HD+

Led by University of Arizona · Updated on 2024-05-07

50

Participants Needed

1

Research Sites

152 weeks

Total Duration

On this page

Sponsors

U

University of Arizona

Lead Sponsor

T

Transdermal Cap, Inc.

Collaborating Sponsor

AI-Summary

What this Trial Is About

Androgenetic alopecia (AGA) is a prevalent disease, occurring in 80% of Caucasian men and 50% of Caucasian women by age 701. Treatments for AGA are limited, and presently the only FDA-approved medications for AGA are topical minoxidil and oral finasteride1. In addition to medical therapies, FDA-cleared medical devices are now utilized for the treatment of AGA as of 20072. These devices, termed low level laser therapy (LLLT), come in multiple forms including combs, helmets and sports cap wearable devices2. These home-use, wearable devices utilize the \~650 nm wavelength laser light to stimulate the hair follicle mitochondria and thereby promote hair growth, a process termed "photobiomodulation"3. Recent meta-analyses investigating photobiomodulation and LLLT for AGA have noted an increase in fluence or energy delivered per cm is associated with increased hair density3. However, randomized control trials (RCT) with direct comparison of LLLT devices of different fluences has yet to be performed. Accordingly, in the present study we aim to investigate if increasing fluence in LLLT devices is associated with increased hair density by comparing sham LaserCap to LaserCap SD (1.15 J/cm2, low fluence) and LaserCap HD+ (3.93 J/cm2, high fluence) in RCT.

CONDITIONS

Official Title

Sham LaserCap vs. LaserCap SD vs. LaserCap HD+

Who Can Participate

Age: 25Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 25 years and older
  • Men and women with androgenetic alopecia, untreated or with 6-month washout of previous treatments
  • Men with Norwood stage IIa to V
  • Women with Ludwig I-1 to II-2, or frontal pattern
  • Fitzpatrick skin types I to IV
Not Eligible

You will not qualify if you...

  • Men with Norwood stage Va, VI, VII
  • Women with Ludwig stage III, advanced
  • Fitzpatrick skin types V and VI
  • Current use or use within past 6 months of other treatments for androgenetic alopecia including topical and oral minoxidil, finasteride, and dutasteride
  • Age below 25 years

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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2
3
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Trial Site Locations

Total: 1 location

1

Banner University Dermatology

Tucson, Arizona, United States, 85719

Actively Recruiting

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Research Team

P

Patrick Jedlowski, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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