Clinical Trial

Aesthetic Improvement of Facial Rhytids Using Injectables

Completed Phase 4
View on ClinicalTrials.gov →
Summary
Revanesse® Renew™+ (Prollenium Medical Technologies Inc.) is a non-crosslinked HA skin booster that combines low- and high-molecular-weight HA at a concentration of 14 mg/mL in a sterile aqueous gel for intradermal injection7. This dual-weight formulation provides both rapid hydration and sustained moisture retention, improving dermal suppleness and promoting subtle textural refinement through physiologic hydration rather than volumization. The present study is designed to compare biweekly and monthly treatment schedules of Revanesse® Renew™+, assessing clinical efficacy, objective biophysical markers, and participant-reported outcomes to inform evidence-based treatment protocols in aesthetic medicine.
Protocol Amendment History 3 changes
critical Trial completed 2026-08-06
notable Primary completion moved earlier: 2027-02-25 -> 2026-06-04 2026-08-06
minor Completion moved earlier: 2027-03-25 -> 2026-08-04 2026-08-06
Trial Details
NCT Number NCT07383766
Lead Sponsor Erevna Innovations Inc.
Conditions Aesthetic
Enrollment 14 participants
Start Date 2026-03-14
Primary Completion 2026-06-04 (estimated)
Study Completion 2026-08-04 (estimated)
Updated on ClinicalTrials.gov 2026-08-05