Clinical Trial

New Technique and Product for Chin Enhancement

Completed
View on ClinicalTrials.gov →
Summary
The use of hyaluronic acid (HA) fillers for soft tissue augmentation offers a valuable treatment modality for the correction of chin retrusion (i.e., when the chin appears to be set back or further back than normal in relation to the rest of the face). Their use is well-tolerated and provides satisfactory aesthetic results by improving facial balance and projection. Although the efficacy of hyaluronic acid HA fillers for chin augmentation has been established, the specific anatomy of the region may lead to adverse events. More specifically, certain fillers with strong integration characteristics may lead to product migration, while others with poor integration characteristics may lead to palpable deformities and distortion of the surrounding injection tissues. Using a filler that has a high concentration of hyaluronic acid, a medium level of firmness and low water absorption may offer an effective option for treating this indication while minimizing certain adverse events. In addition, using consistent, standardized injection techniques can help achieve an ideal result. We believe that the use of a novel HA gel (Revanesse Sculp+) for the chin, with a high concentration of HA, a moderate firmness and low water absorption, will perform better than historical controls with firmer properties in the management of chin retrusion.
Protocol Amendment History 2 changes
critical Trial completed 2026-08-06
minor Completion pushed: 2026-06-24 -> 2026-07-24 2026-08-06
Trial Details
NCT Number NCT07193199
Lead Sponsor Erevna Innovations Inc.
Conditions Aesthetic
Enrollment 21 participants
Start Date 2025-06-02
Primary Completion 2026-06-01 (estimated)
Study Completion 2026-07-24 (estimated)
Updated on ClinicalTrials.gov 2026-08-05