Trials / Completed
CompletedNCT00935272
Safety/Efficacy Study of Restylane® in Lip Augmentation
A Randomized, Evaluator-Blinded, No-Treatment-Controlled Study of the Effectiveness and Safety of Restylane® in the Augmentation of Soft Tissue Fullness of the Lips
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 180 (actual)
- Sponsor
- Medicis Global Service Corporation · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
To determine the safety and effectiveness of Restylane® when used for lip augmentation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Restylane® | Restylane® injections in the lips |
| DEVICE | Non-Treatment | Non- Treatment |
Timeline
- Start date
- 2009-07-01
- Primary completion
- 2010-06-01
- Completion
- 2010-07-01
- First posted
- 2009-07-09
- Last updated
- 2012-01-30
- Results posted
- 2012-01-30
Locations
12 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00935272. Inclusion in this directory is not an endorsement.