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

RecruitingNAAges 40 Years - 70 YearsAllLynch Regenerative Medicine
NCT07718347 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
Inclusion Criteria -:Adults 40-65 70 years * Glogau III-IV * Fitzpatrick II-IV. * Suitable for ablative laser * non-smoker ≥ 3 years * Willing to comply with post-procedure regimen * patient reported outcome documentation, and photo documentation. Exclusion Criteria: * Fitzpatrick I or \> IV, * recent facial procedures (\< 6 months) * active skin disease * pregnancy/lactation * implanted devices * history of keloids.
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What it tests

  • ariessence pure PDGF+™ is a sterile aqueous formulation containing Hyaluronic Acid and pure platelet-derived growth factor (PDGF).
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Where

2 sites
Laser & Skin Surgery Medical Group
Sacramento, United States
The Practice of Brian S. Biesman, MD
Nashville, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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