Safety and Effectiveness of Mosaic for the Treatment of Midface Volume Deficit
NCT: NCT07710443 · RECRUITING
Brief Summary
The goal of this clinical trial is to study whether the Mosaic Injectable Dermal Implant is a safe and effective treatment for age-related midface volume deficit in adults who are at least 22 years of age. The main questions it aims to answer are: 1. What medical problems do participants have when receiving Mosaic over the 12 months following treatment. 2. How much does Mosaic improve the midface volume at 6 months post-treatment. Participants will: Receive injections to the midface to correct volume deficit. One month from initial injection, if the doctor decides that touch-up injections are required, further injections may be received. Participants will visit the clinic following each injection and at 3, 6 and 12 months post-treatment to have photos taken of their face as a record of their midface volume. Participants will also keep a diary for 30 days following each treatment so that they can record any symptoms that may be linked to the treatment.
Frequently Asked Questions
What is Safety and Effectiveness of Mosaic for the Treatment of Midface Volume Deficit?
Safety and Effectiveness of Mosaic for the Treatment of Midface Volume Deficit is a clinical trial registered under NCT07710443. Current status: RECRUITING.
What is the status of NCT07710443?
The current status of NCT07710443 (Safety and Effectiveness of Mosaic for the Treatment of Midface Volume Deficit) is: RECRUITING.
When did Safety and Effectiveness of Mosaic for the Treatment of Midface Volume Deficit start?
Safety and Effectiveness of Mosaic for the Treatment of Midface Volume Deficit started on 2026-09-08.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.