Clinical Trials Directory

Trials / Completed

CompletedNCT06336135

Reduction in Symptoms After Laser Therapy With Acorn aHFS

A Prospective, Single-blind, Randomized, Placebo-controlled, Clinical Trial Evaluating Reduction in Severity and Duration of Symptoms After Laser Therapy With Acorn aHFS

Status
Completed
Phase
Study type
Observational
Enrollment
11 (actual)
Sponsor
Acorn Biolabs Inc. · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

This study evaluates the severity and duration of symptoms experienced after laser therapy comparing four post-procedure topical products. Each product is applied to an individual region of interest (5 cm diameter) on the back or décolleté according to randomization code after laser therapy. The subject, blind to the product applied to each of 4 regions of interest, assesses eight symptoms daily for 14 days. Photography is performed daily.

Conditions

Interventions

TypeNameDescription
OTHERautologous hair follicle derived secretomeaHFS is a cosmetic topical intended to be applied to the human body after skin resurfacing cosmetic procedures. aHFS is produced from the plucked hair follicles of each individual, making it autologous.

Timeline

Start date
2024-03-25
Primary completion
2025-12-02
Completion
2025-12-02
First posted
2024-03-28
Last updated
2025-12-12

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT06336135. Inclusion in this directory is not an endorsement.