Autologous Hair Follicle Derived Secretome as Adjunct to Aesthetic Procedures

Acorn Biolabs

Status: Enrolling

Conditions: Post Procedural Erythema

Study type: Observational

Funder types: Industry

Identifiers

NCT06477172

ACN-101

Details and patient eligibility

About

Non-interventional, multi-site, prospective, open-label, observational, real-world study of autologous hair follicle secretome use.

Full description

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.

Enrollment: 500 estimated patients

Sex: All

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Male and Female

• Ages: 18-60

• Any Fitzpatrick skin type

• Planning a medical aesthetic procedure

• For subjects receiving hair procedures:

  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
  2. Microneedling of the face (roller, stamper, radiofrequency or pen) or Tixel of the face
  3. Microneedling of the scalp (roller, stamper or pen for hair loss) or Keralase of the scalp
  4. 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

Exclusion criteria

• 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