Trials / Completed
CompletedNCT00407914
Safety and Effectiveness of Aquamid as Compared to Restylane for the Aesthetic Treatment of Nasolabial Folds
A Double-Masked, Randomized, Multi-Center, 2-Arm Parallel Study Comparing the Safety and Effectiveness of Aquamid and Restylane for the Aesthetic Treatment of Nasolabial Folds
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 315 (actual)
- Sponsor
- Contura · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to compare the effectiveness of Aquamid and Restylane in aesthetically enhancing nasolabial folds 6 months after treatment and to evaluate the safety of Aquamid through 12 months after treatment. The study includes an extended follow up to 24 months.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Aquamid | Subcutaneous injection |
| DEVICE | Restylane | Injection in dermis |
Timeline
- Start date
- 2006-12-01
- Primary completion
- 2008-08-01
- Completion
- 2009-07-01
- First posted
- 2006-12-05
- Last updated
- 2009-10-08
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00407914. Inclusion in this directory is not an endorsement.