Clinical Trials Directory

Trials / Completed

CompletedNCT05777759

Safety and Effectiveness of Restylane Lyft With Lidocaine for Augmentation of the Chin Region to Improve the Chin Profile

A Randomized, Evaluator-blinded, Parallel Group, Comparator-controlled, Multicenter Study to Evaluate the Safety and Effectiveness of Restylane Lyft With Lidocaine for Augmentation of the Chin Region to Improve the Chin Profile

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
174 (actual)
Sponsor
Galderma R&D · Industry
Sex
All
Age
22 Years
Healthy volunteers
Accepted

Summary

The primary objective of the study is to demonstrate non-inferiority of Restylane Lyft with Lidocaine versus a comparator-control for augmentation of the chin region to improve the chin profile.

Conditions

Interventions

TypeNameDescription
DEVICERestylane Lyft with Lidocainehyaluronic acid
DEVICEJuvederm Voluma XChyaluronic acid

Timeline

Start date
2023-03-22
Primary completion
2023-11-11
Completion
2024-07-08
First posted
2023-03-21
Last updated
2025-01-17

Locations

12 sites across 2 countries: United States, Puerto Rico

Regulatory

Source: ClinicalTrials.gov record NCT05777759. Inclusion in this directory is not an endorsement.

Safety and Effectiveness of Restylane Lyft With Lidocaine for Augmentation of the Chin Region to Improve the Chin Profil (NCT05777759) · Clinical Trials Directory