Restylane Lyft with Lidocaine for Chin Augmentation

Not yet recruiting at 7 trial locations
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of 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.

Are You a Good Fit for This Trial?

Inclusion Criteria

I am male or a non-pregnant, non-breastfeeding female, and I am at least 22 years old.
I want treatment to enhance or correct my chin shape.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Initial Treatment

Participants receive initial treatment with Restylane Lyft with Lidocaine in the chin region at Baseline

1 month
1 visit (in-person)

Touch-up Treatment (optional)

Participants may receive an optional touch-up treatment 1 month after initial treatment

1 month
1 visit (in-person)

Retreatment (optional)

Participants may receive an optional retreatment 12 months after the last treatment

12 months
1 visit (in-person)

Follow-up

Participants are monitored for safety and effectiveness after the optional retreatment

3 months
1 visit (in-person)

What Are the Treatments Tested in This Trial?

Interventions

  • Restylane Lyft with Lidocaine

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Dermal Filler for Indication: Restylane Lyft with LidocaineExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Galderma R&D

Lead Sponsor

Trials
303
Recruited
60,700+
Flemming Ørnskov profile image

Flemming Ørnskov

Galderma R&D

Chief Executive Officer since 2019

MD, MPH

Baldo Scassellati Sforzolini profile image

Baldo Scassellati Sforzolini

Galderma R&D

Chief Medical Officer

MD, PhD