Trials / Completed
CompletedNCT01671839
Study of the Cabochon System for Improvement in the Appearance of Cellulite
Pivotal Study of the Cabochon System for Improvement in the Appearance of Cellulite
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 55 (actual)
- Sponsor
- Merz North America, Inc. · Industry
- Sex
- Female
- Age
- 18 Years – 55 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate the safety and effectiveness of the Cabochon System for the improvement in the appearance of cellulite.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Subcutaneous tissue release with the Cabochon System | Device: Subcutaneous tissue release |
Timeline
- Start date
- 2012-08-01
- Primary completion
- 2013-09-01
- Completion
- 2015-12-01
- First posted
- 2012-08-24
- Last updated
- 2019-12-10
- Results posted
- 2014-09-04
Locations
3 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT01671839. Inclusion in this directory is not an endorsement.