Study to Evaluate the Safety of Retreatment With Restylane® Lyft With Lidocaine for Augmentation of the Chin Region
Starting soon · Not applicable
Conditions studied: Chin Augmentation
In brief
The primary objective of this study is to evaluate the safety of Restylane Lyft with Lidocaine for augmentation of the chin region 3 months after retreatment.
Key facts
- Study ID
- NCT07566286
- Run by
- Galderma R&D
- People needed
- 100
- Starts
- 2026-06-03
- Expected to finish
- 2028-02-28
- Last updated by the study team
- 2026-07-01
Who can join
Age: 22 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Males or non-pregnant, non-breastfeeding females, 22 years of age or older.
- Intent to receive treatment for augmentation and correction of retrusion in the chin region.
You may not qualify if…
- Known/previous allergy or hypersensitivity to any injectable hyaluronic acid (HA) gel or to gram positive bacterial proteins.
- Known/previous allergy or hypersensitivity to local anesthetics, e.g. lidocaine or other amide-type anesthetics.
- Previous or present multiple allergies or severe allergies, such as manifested by anaphylaxis or angioedema, or family history of these conditions.
- Previous facial surgery (including facial aesthetic surgery and liposuction), below the level of the horizontal line from subnasale.
- Any previous aesthetic procedures or implants.
- Presence of any disease or lesions near or on the area to be treated.
Where it is running
- Galderma Investigational Site # 8680 — Westport, Connecticut, United States
- Galderma Investigational Site # 8774 — Boynton Beach, Florida, United States
- Galderma Investigational Site # 7030 — Coral Gables, Florida, United States
- Galderma Investigational Site # 8682 — Coral Gables, Florida, United States
- Galderma Investigational Site # 7042 — Atlanta, Georgia, United States
- Galderma Investigational Site # 7043 — Bethesda, Maryland, United States
- Galderma Investigational Site # 7118 — Nashville, Tennessee, United States
- Galderma Investigational Site # 8662 — Spring, Texas, United States
Full record on ClinicalTrials.gov
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