Trials / Completed
CompletedNCT03174132
Pain and Safety of Restylane Perlane With and Without Lidocaine for Correction of Moderate and Severe Nasolabial Folds
A Randomised, Multi-center, Subject and Evaluator-blinded Study Comparing the Pain and the Safety Profile Associate With Correction of Moderate to Severe Nasolabial Folds Using Restylane Perlane Lidocaine Compared to Restylane Perlane
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 70 (actual)
- Sponsor
- Galderma R&D · Industry
- Sex
- All
- Age
- 20 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the pain and safety in associated with injection of Restylane Perlane Lidocaine compared to Restylane Perlane using VAS scale
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Restylane Perlane Lidocaine | Intradermal injection |
| DEVICE | Restylane Perlane | Intradermal injection |
Timeline
- Start date
- 2017-09-21
- Primary completion
- 2018-01-16
- Completion
- 2018-01-16
- First posted
- 2017-06-02
- Last updated
- 2022-08-26
- Results posted
- 2019-09-20
Locations
3 sites across 1 country: Taiwan
Source: ClinicalTrials.gov record NCT03174132. Inclusion in this directory is not an endorsement.