A Study to Evaluate the Safety and Efficacy of Restylane Defyne for Chin Augmentation and Correction of Chin Retrusion

Completed · Not applicable

Conditions studied: Chin Retrusion, Chin Augmentation

In brief

To demonstrate the effectiveness of Restylane Defyne for chin augmentation and correction of chin retrusion by demonstrating the superiority in responder rates relative to no treatment.

Key facts

Study ID

NCT03624816

Run by

Galderma R&D

People needed

140

Starts

2018-08-21

Expected to finish

2020-02-20

Last updated by the study team

2022-10-06

Who can join

Age: 22 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Subjects willing to comply with the requirements of the study and providing a signed written informed consent.
• Males or non-pregnant, non-breastfeeding females, 22 years of age or older, seeking chin augmentation or correction of retrusion

You may not qualify if…

• Allergy of hypersensitivity to any injectable hyaluronic acid gel or to gram positive bacterial proteins
• Allergy or hypersensitivity to lidocaine or other amide-type anesthetics, or topical anesthetics or nerve blocking agents

Where it is running

• Westside Aesthetics — Los Angeles, California, United States
• Ablon Skin Institute and Research Center — Manhattan Beach, California, United States
• Marcus Facial Plastic Surgery — Redondo Beach, California, United States
• Moradi M.D. — Vista, California, United States
• Skin Research Institute, LLC — Coral Gables, Florida, United States
• Etre Cometic Dermatology and Laser Center — New Orleans, Louisiana, United States
• WIDLS Chevy Chase — Chevy Chase, Maryland, United States
• Maryland Laser Skin and Vein Institute — Hunt Valley, Maryland, United States
• Union Square Laser Dermatology — New York, New York, United States
• Wilmington Dermatology and Laser Center — Wilmington, North Carolina, United States
• Dallas Plastic Surgery Institute — Dallas, Texas, United States

Full record on ClinicalTrials.gov

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