Trials / Completed
CompletedNCT00823069
Safety Study That Compares Perlane to Perlane With Lidocaine (Perlane-L) While Correcting Wrinkles in the Area Around Your Nose
A Randomized, Double-Blind Study Comparing Safety and Tolerability of Perlane® With and Without Addition of 0.3% Lidocaine HCL During Correction of Nasolabial Folds
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Medicis Global Service Corporation · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
Safety study that compares Perlane to Perlane with Lidocaine while correcting wrinkles in the area around your nose.
Detailed description
This is a split-face design. All 60 subjects receive Perlane on one side of their face, and Perlane-L on the other. Subjects and the investigator is blinded to which side of face receives which product. These are one time injections.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Perlane and Perlane-L | This is a split face design and each subject received both Perlane-L and Perlane. Treatments were blinded, randomized, and successive. |
Timeline
- Start date
- 2009-01-01
- Primary completion
- 2009-03-01
- Completion
- 2009-04-01
- First posted
- 2009-01-15
- Last updated
- 2010-11-30
- Results posted
- 2010-11-30
Locations
3 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00823069. Inclusion in this directory is not an endorsement.