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Study identifier: NCT07718347 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Post-market Cosmetic Evaluation of Ariessence™ Pure PDGF+ Following Ablative Laser

Condition: Immediate Post-Treatment Care · Aging Mid-Face · Aging  ·  Sponsor: Lynch Regenerative Medicine

PhaseNA
Planned participants21
Who can joinAll sexes, 40 Years to 70 Years
Healthy volunteersNo

About this study

ariessence is intended to be used as a viscous, leave-on solution designed for topical application to the face. It is intended to be used following non-medical cosmetic procedures, performed by licensed healthcare professionals to enhance comfort and maintain skin hydration. This study is designed to be a multi-center, post-market cosmetic evaluation of ariessence applied to the full face after an ablative laser procedure to evaluate improvements in procedure tolerability and improvements in the appearance of the skin, compared to an emollient control.

This description comes directly from the study's public registry record.

Talk to the study team

Josh Arnold  ·  302-604-4532  ·  clinicaltrials@purity-health.com

Always discuss trial participation with your own doctor first.

Locations (2)

Laser & Skin Surgery Medical GroupSacramento, California, United StatesRecruiting
The Practice of Brian S. Biesman, MDNashville, Tennessee, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07718347