Hydraderm for Androgenic Alopecia (NCT05426629) | Clinical Trial Compass
WithdrawnPhase 4
Hydraderm for Androgenic Alopecia
Stopped: IRB closed
United States0Started 2022-03-14
Plain-language summary
The study will be focused on evaluating the use of hydradermabrasion on the scalp. The study aims to assess the effect of this treatment on scalp health and hair growth.
Who can participate
Age range18 Years – 65 Years
SexALL
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Inclusion Criteria:
* Participants who can give voluntary, written informed consent to participate in this study and from whom consent has been obtained including HIPAA Authorization
* Participants who have androgenetic alopecia
* Healthy men and women, ages 18 - 65 years of age
* Participants who understand the study and can follow study instructions and are willing to attend the required study visits
* Participants who agree to be photographed for research purposes and their identity may not be concealed in these photographs.
* Participants who agree to continue their same treatment they are on at the baseline visit for androgenetic alopecia, for the entire duration of the study without plans to stop, change or add additional treatments.
* Participants who agree to use the same shampoo for the duration of the study
Exclusion Criteria:
* Participants who have not had a change to hair loss treatment for 4 months prior to study enrollment
* Participants who have an active or known skin inflammation or infection within the treatment area.
* Participants who have an active or known acute skin allergies
* Participants who have any other scalp conditions including eczema, psoriasis, infection, or scars within the treatment area
* Participants of child-bearing potential who are not using an approved method of birth control (oral contraceptives, IUD, contraceptive implant, barrier methods with spermicide or abstinence). Females of non-childbearing potential are defined as post-me…