Completed
NCT Number: NCT02636894
Evaluation of the Efficacy of Restylane Silk in the Treatment of Cheek Fold (Radial Smile Lines)
Filler study for smile lines in cheek folds
Completed
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Notify MeKey information
Conditions
Age range
21 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
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
Treatment and study plan
Primary outcomes
-
Evaluation of the Efficacy of Restylane Silk in the Treatment of Cheek folds (Radial Smile Lines)
Time frame: 6 months
Improvement of subjects based on 5 point global aesthetic scale (GAIS)
Sponsors and collaborators
Lead sponsor
Amanda D. Spear, CCRC
Other
Registry information
Important dates
- Study start
- 2016
- Primary completion
- 2016
- Study completion
- 2016
- First posted
- Dec 22, 2015
- Registry last updated
- Mar 27, 2019
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.