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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04897555
Other study ID # IRE0219
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2019
Est. completion date October 1, 2019

Study information

Verified date May 2021
Source Freedom Laser, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this research is to study the ongoing effectiveness of a light therapy device for human hair growth. This device, called the iRestore Eyebrow Device, is a type of cold, or non-heat producing light therapy system that will emit light on the hair growth cells within and around the hair follicle. When these cells do not function properly, one may experience common problems such as baldness and thinning or brittle hair. The application of a special category of low-level light to be studied in the project may cause an increase in essential nutrients to the damaged hair follicles and skin cells, leading to a reduction in hair loss and in some cases, possibly leading to re-growth.


Description:

This study on LLLT aims to define the safety and physiologic effects that occur when the human hair follicle and surrounding tissue structures are exposed to this type of radiation. Thus far, all reports on the efficacy of laser light and LED light in this area, have been, in large part, unsupported by multi-center, randomized, double blind, controlled studies. To properly identify the effects in human subjects, exposure to LLLT is not sufficient. The analysis of the non-radiated and radiated tissues is required to elucidate the tissue response and efficacy of the laser therapy. The theory that is widely accepted is that the mitochondria are the powerhouse of the stem cells that cause hair growth. The LLLT "turns on" the nutrient pump process that energizes the mitochondria, which leads to an increase in ATP and subsequent reversal of hair follicles from the dormant stage of growth called telogen, to the active growth stage called anagen.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date October 1, 2019
Est. primary completion date August 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Female subjects experiencing any type of non-traumatic eyebrow hair loss. - Apparent good health. Exclusion Criteria: - Previous involvement in other eyebrow hair studies. - Use of any hair growth agent within the last 4 weeks. - Evidence of any current viral, fungal or bacterial infection.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
LLLT
This is a low-level light (LED) device configured in the shape of a headband, operating at 650 +/-10 nanometers and 940 +/- 10 nanometers, that contains 12 of each wavelength for a total of 24 LEDs.

Locations

Country Name City State
United States Bodian Dermatology Great Neck New York
United States NST Consultants, Inc. Mendham New Jersey

Sponsors (1)

Lead Sponsor Collaborator
Freedom Laser Therapy, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in number of terminal hairs Pre & Post treatment terminal hair counts 12 weeks
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