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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
University of Arizona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Androgenetic Alopecia

Eligibility Criteria

25 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

    First Posted
    May 4, 2022
    Last Updated
    May 4, 2022
    Sponsor
    University of Arizona
    Collaborators
    Transdermal Cap, Inc.
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    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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