This non-interventional, observation study is to collect real-world data on the use of an autologous, hair follicle derived secretome topical cosmetic product following various medical aesthetic procedures.
Age
18–any
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Male and Female
Ages: 18-60
Any Fitzpatrick skin type
Planning a medical aesthetic procedure
For subjects receiving hair procedures (closed to enrollment):
1. Androgenic alopecia
2. Traction alopecia
3. Scarring alopecia
4. Stable use of any medication or supplement for hair loss, including finasteride, any other 5 α-reductase inhibitor, minoxidil, steroids, or hormonal products, during the 3 months prior to enrollment in the study is allowed.
5. No intention to start new hair growth medications or change dose of hair growth medications from the time of consent through the end of the study follow-up period.
Undergoing one of the following medical aesthetic procedures:
1. Laser resurfacing of the face (ablative or non-ablative) or Ellacor of the face (Ellacor closed to enrollment)
2. Tixel of the face
3. Keralase of the scalp (scalp treatment closed to enrollment)
4. Acne Scars and Surgery scars, either old or new as long as old scars are also being treated with ablative or non-ablative laser or microneedling (e.g. abdominoplasty, breast reduction/ reconstruction/enhancement, post-weight loss, etc.
Planning to use Acorn Autologous Hair Follicle Secretome cosmetic product
You may not be if
Pregnant or Breastfeeding
Participation in an interventional clinical trial in the last 30 days
Use of other topical cosmetic products that may confound results
Use of retinoids within 7 days prior to facial procedure
For those receiving hair treatment, must not have had a hair transplant in the treatment area within the past 12 months
Any health condition that in the investigator's opinion should preclude participation in study
