Sham LaserCap vs. LaserCap SD vs. LaserCap HD+
Primary Purpose
Androgenetic Alopecia
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
LaserCap SD
Sham LaserCap
LaserCap HD+
Sponsored by
About this trial
This is an interventional treatment trial for Androgenetic Alopecia
Eligibility Criteria
Inclusion criteria:
- 25 years and older
- Men and women with AGA, untreated or with 6-month washout of previous treatments
- Men: Norwood stage IIa - V
- Women: Ludwig I-1 - II-2, or frontal pattern
- All patients: Fitzpatrick skin types I to IV
Exclusion criteria:
- Men: Norwood stage Va, VI, VII
- Women: Ludwig stage III, advanced
- All patients: Fitzpatrick skin types V, VI
- Current use or within the past six month of other treatment for AGA, including topical and oral minoxidil, topical and oral finasteride and dutasteride
- Age 0-25 years
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Sham Comparator
Experimental
Experimental
Arm Label
Sham LaserCap
Lasercap SD
Lasercap HD+
Arm Description
Sham device
Low fluence LLLT
High fluence LLLT
Outcomes
Primary Outcome Measures
Target area total hair count at 26 weeks via phototrichogram
Secondary Outcome Measures
Target area vellus hair count at 26 weeks via phototrichogram
Target area terminal hair count at 26 weeks via phototrichogram
Physician assessed improvement via global photography at 26 weeks
Hair growth rate at 26 weeks via phototrichogram
Full Information
NCT ID
NCT05365360
First Posted
May 4, 2022
Last Updated
May 4, 2022
Sponsor
University of Arizona
Collaborators
Transdermal Cap, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT05365360
Brief Title
Sham LaserCap vs. LaserCap SD vs. LaserCap HD+
Official Title
Effect of Increasing Fluence on Efficacy of Low Level Laser Therapy for Androgenetic Alopecia, a Randomized Control Trial
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 2022 (Anticipated)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
August 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Arizona
Collaborators
Transdermal Cap, Inc.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
5. Study Description
Brief Summary
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Androgenetic Alopecia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Sham LaserCap
Arm Type
Sham Comparator
Arm Description
Sham device
Arm Title
Lasercap SD
Arm Type
Experimental
Arm Description
Low fluence LLLT
Arm Title
Lasercap HD+
Arm Type
Experimental
Arm Description
High fluence LLLT
Intervention Type
Device
Intervention Name(s)
LaserCap SD
Intervention Description
LaserCap SD
Intervention Type
Device
Intervention Name(s)
Sham LaserCap
Intervention Description
Sham LaserCap
Intervention Type
Device
Intervention Name(s)
LaserCap HD+
Intervention Description
LaserCap HD+
Primary Outcome Measure Information:
Title
Target area total hair count at 26 weeks via phototrichogram
Time Frame
26 weeks
Secondary Outcome Measure Information:
Title
Target area vellus hair count at 26 weeks via phototrichogram
Time Frame
26 weeks
Title
Target area terminal hair count at 26 weeks via phototrichogram
Time Frame
26 weeks
Title
Physician assessed improvement via global photography at 26 weeks
Time Frame
26 weeks
Title
Hair growth rate at 26 weeks via phototrichogram
Time Frame
26 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion criteria:
25 years and older
Men and women with AGA, untreated or with 6-month washout of previous treatments
Men: Norwood stage IIa - V
Women: Ludwig I-1 - II-2, or frontal pattern
All patients: Fitzpatrick skin types I to IV
Exclusion criteria:
Men: Norwood stage Va, VI, VII
Women: Ludwig stage III, advanced
All patients: Fitzpatrick skin types V, VI
Current use or within the past six month of other treatment for AGA, including topical and oral minoxidil, topical and oral finasteride and dutasteride
Age 0-25 years
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Patrick Jedlowski, MD
Phone
(520) 694-8888
Email
pjedlowski@email.arizona.edi
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Sham LaserCap vs. LaserCap SD vs. LaserCap HD+
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