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

A

Amanda D. Spear, CCRC

Status

Completed

Conditions

Smile Lines

Treatments

Device: Restylane Silk

Study type

Interventional

Funder types

Other

Identifiers

NCT02636894
Restylane Silk

Details and patient eligibility

About

Filler study for smile lines in cheek folds

Enrollment

30 patients

Sex

All

Ages

21 to 65 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Restylane Silk
Other group
Description:
Restylane Silk
Treatment:
Device: Restylane Silk

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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