Autologous Hair Follicle Derived Secretome as Adjunct to Aesthetic Procedures
ConditionPost Procedural Erythema
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAcorn Biolabs Inc.
About this trial
Non-interventional, multi-site, prospective, open-label, observational, real-world study of autologous hair follicle secretome use.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Male and Female
Ages: 18-60
Any Fitzpatrick skin type
Planning a medical aesthetic procedure
Disqualifiers
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
Trial population
The study population will be patients planning a medical aesthetic procedure and use of Autologous Hair Follicle Secretome cosmetic post-procedure.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Post-Procedure Symptoms
Symptoms of redness, swelling, oozing, pain, tenderness, crusting, itching and discoloration will be measured using a 1-10 likert scale with 0 being best possible and 10 being worst imaginable.
Time frame
1-7 days2
Downtime Questionnaire
Questionnaire asking what activities would they have done, if it were not for their face appearance. Date of end of downtime captured.
Time frame
1-7 daysSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov