Trials / Completed
CompletedNCT02340091
A Clinical Study to Evaluate the Efficacy and Safety of YVOIRE Classic Plus Versus YVOIRE Classic 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 Plus Versus HA IDF 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 plus (with lidocaine) injected in the nasolabial fold compared to HA IDF (without lidocaine).
Detailed description
The objective of this study was to confirm the superiority of HA IDF II plus (with lidocaine) injected in the nasolabial fold compared to HA IDF II (without lidocaine) in the improvement of local pain and evaluate the wrinkle-correcting effect, GAI and safety.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | HA IDF plus | |
| DEVICE | HA IDF |
Timeline
- Start date
- 2014-02-01
- Primary completion
- 2014-06-01
- Completion
- 2015-06-01
- First posted
- 2015-01-16
- Last updated
- 2019-01-23
- Results posted
- 2019-01-23
Source: ClinicalTrials.gov record NCT02340091. Inclusion in this directory is not an endorsement.