Actively Recruiting
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
Eligibility Criteria
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
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
Trial Site Locations
Total: 1 location
1
Banner University Dermatology
Tucson, Arizona, United States, 85719
Actively Recruiting
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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