Trials / Completed
CompletedNCT02558283
A Safety and Efficacy Study of JUVÉDERM® VOLIFT® With Lidocaine and Restylane® for Nasolabial Folds in Chinese Adults
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 175 (actual)
- Sponsor
- Allergan · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a safety and efficacy study of JUVÉDERM® VOLIFT® with Lidocaine and Restylane® in Chinese adults with nasolabial folds.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | JUVÉDERM® VOLIFT® with Lidocaine | JUVÉDERM® VOLIFT® with lidocaine injected into the nasolabial fold on Day 1, with optional touch-up injections into the nasolabial fold on Month 1. |
| DEVICE | Restylane® | Restylane® injected into the nasolabial fold on Day 1, with optional touch-up injections into the nasolabial fold on Month 1. |
Timeline
- Start date
- 2016-01-25
- Primary completion
- 2017-06-19
- Completion
- 2017-06-19
- First posted
- 2015-09-23
- Last updated
- 2017-08-30
Locations
5 sites across 1 country: China
Source: ClinicalTrials.gov record NCT02558283. Inclusion in this directory is not an endorsement.