Alopecia Clinical Trial
Official title:
Evaluation of Low Level Light Therapy (LLLT) as a Primary Therapy for Non-Specific Alopecia of the Eyebrow in Women
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 |
Verified date | May 2021 |
Source | Freedom Laser, Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
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. |
Country | Name | City | State |
---|---|---|---|
United States | Bodian Dermatology | Great Neck | New York |
United States | NST Consultants, Inc. | Mendham | New Jersey |
Lead Sponsor | Collaborator |
---|---|
Freedom Laser Therapy, Inc. |
United States,
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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