Clinical Research Directory

Efficacy of an LED Mask

The goal of this interventional study is to evaluate the efficacy and perception a commercial LED device in 110 healthy adult females and males between the ages of 35-65 years old, inclusively. The main questions it aims to answer are: Does daily use of this commercial LED device improve overall skin appearance as measured by clinical tools (expert clinical grading, cutometer, digital photography, and VISIA-CR? Does daily use of this commercial LED device improve subjective skin appearance? Is daily use of this commercial LED device well tolerated? Participants will complete a 9-minute LED treatment (4.5 minutes LED, 4.5 minutes LED+ infrared light therapy) with a commercially available device every day for 12 weeks. They will visit the clinic three times (baseline, 6 weeks, 12 weeks) for clinical grading of skin.

AnteAGE Biosomes With Radiofrequency Microneedling for Facial Skin Rejuvenation

This prospective, randomized controlled study evaluated the efficacy and tolerability of AnteAGE Biosome Solution used in conjunction with facial radiofrequency microneedling. Eligible participants with facial rhytids and/or uneven skin tone and texture were randomized 1:1 to an active treatment group or a control group. All participants underwent facial radiofrequency microneedling. Participants in the active group received AnteAGE Biosome Solution during treatment and an AnteAGE skincare regimen, while control participants received hyaluronic acid as the treatment glide and control skincare products. Clinical outcomes included standardized facial photography, investigator assessments, Global Aesthetic Improvement Scale assessments, participant-reported outcomes, and assessment of adverse reactions and post-procedure healing through Day 60.