Evaluation of the Efficacy of Restylane Silk in the Treatment of Cheek Fold (Radial Smile Lines)

N/ACompletedNCT02636894

Amanda D. Spear, CCRC30 enrolled

Overview

Filler study for smile lines in cheek folds

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Smile Lines

Interventions

Restylane SilkDEVICE

Eligibility

Sex: ALLMin age: 21 YearsMax age: 65 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Male or female between 21-65 years of age * Willing to comply with study visits and procedures * Willingness to refrain form surgical, laser, or injectable treatments in cheek region during study Exclusion Criteria: * History of trauma, acne scarring, burns, or other changes to skin in treatment area * Use of botulinum toxin in the lateral cheeks/perioral region in past 6 months * Use of injectable fillers in the lateral cheeks/perioral within last 2 years * History of facelift in the last year * History of facial nerve palsy

Outcomes

Primary Outcomes

Evaluation of the Efficacy of Restylane Silk in the Treatment of Cheek folds (Radial Smile Lines)

Improvement of subjects based on 5 point global aesthetic scale (GAIS)

Time frame: 6 months

Data from ClinicalTrials.gov

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