Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07383766

Aesthetic Improvement of Facial Rhytids Using Injectables

A Prospective Clinical Study Evaluating the Effects of a Skin Boosting Injectable on the Aesthetic Improvement of Facial Rhytids

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
14 (estimated)
Sponsor
Erevna Innovations Inc. · Academic / Other
Sex
All
Age
30 Years – 75 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICERevanesse® Renew™+Revanesse® Renew™+, a sterile, colorless, odorless, transparent, aqueous gel of synthetic origin supplied in pre-filled disposable syringes. Revanesse® Renew™+ is manufactured by Prollenium Medical Technologies Inc. It consists of both low- and high-molecular-weight hyaluronic acid (HA) at a concentration of 14 mg/mL. The product is supplied in pre-filled disposable syringes, each containing 1.2 mL of ready-to-use gel intended for single use. The product does not require reconstitution or dilution prior to injection and is administered directly into the superficial to mid-dermal plane according to the manufacturer's instructions.

Timeline

Start date
2026-02-25
Primary completion
2027-02-25
Completion
2027-03-25
First posted
2026-02-03
Last updated
2026-02-05

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT07383766. Inclusion in this directory is not an endorsement.