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Autologous Hair Follicle Derived Secretome as Adjunct to Aesthetic Procedures

A

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

No Healthy Volunteers

Inclusion criteria

  • Male and Female,
  • Ages: 18-60
  • Any Fitzpatrick skin type
  • Planning a medical aesthetic procedure
  • Planning to use aHFS 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
  • Any health condition that in the investigator's opinion should preclude participation in study

Trial contacts and locations

24

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Central trial contact

Lisa Campbell, PhD

Data sourced from clinicaltrials.gov

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