Trials / Completed
CompletedNCT02340078
A Clinical Study to Evaluate the Efficacy and Safety of YVOIRE Volume Plus Versus YVOIRE Volume in Nasolabial Fold Injection
A Randomized, Multi Center, Double-blind, Active-controlled, Matched Pairs Design Clinical Study to Evaluate the Efficacy and Safety of HA IDF II Plus Versus HA IDF II in Nasolabial Fold Injection
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 62 (actual)
- Sponsor
- LG Life Sciences · Industry
- Sex
- Female
- Age
- 30 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study was to evaluate the efficacy and safety of HA IDF II plus (with lidocaine) injected in the nasolabial fold compared to HA IDF II (without lidocaine).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | HA IDF II plus | |
| DEVICE | HA IDF II |
Timeline
- Start date
- 2013-11-01
- Primary completion
- 2015-02-01
- Completion
- 2015-02-01
- First posted
- 2015-01-16
- Last updated
- 2019-01-23
- Results posted
- 2019-01-23
Source: ClinicalTrials.gov record NCT02340078. Inclusion in this directory is not an endorsement.