Hydraderm for Androgenic Alopecia

  • End date
    Mar 21, 2024
  • participants needed
  • sponsor
    University of Minnesota
Updated on 8 July 2022
androgenic alopecia


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.

Condition Androgenic Alopecia
Treatment Venus Glow
Clinical Study IdentifierNCT05426629
SponsorUniversity of Minnesota
Last Modified on8 July 2022


Yes No Not Sure

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-menopausal (absence of menstrual bleeding for one year), hysterectomy, or bilateral oophorectomy
Participants who are pregnant, planning to become pregnant or breastfeeding. A urine pregnancy test will be done to rule out pregnancy
Participants who are HIV+ / Hepatitis B + / Hepatitis C+
Participants who have been diagnosed or have a known history of any hematopathology disorders
Participants who have been diagnosed or have a known history of haemostasis disorders
Participants who have been diagnosed or have a known history of an autoimmune diseases
Participants who are undergoing chemotherapy
Participants with a history of any skin cancer on the scalp
Participants who have had skin biopsy or procedure on scalp in last month
Participants who have an implantable devices such as a deep brain stimulator in or other implantable device on or near treatment area
Non-English speakers
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What happens next?
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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