About this trial
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.
Eligibility criteria
Qualifiers
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.
Disqualifiers
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.
Trial design
Treatments tested in this trial
- Restylane Lyft with Lidocaine