Trials / Completed
CompletedNCT02873104
Pivotal Study of the truSculpt Radiofrequency Device for Circumferential Reduction
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 70 (actual)
- Sponsor
- Cutera Inc. · Industry
- Sex
- All
- Age
- 24 Years – 60 Years
- Healthy volunteers
- Accepted
Summary
To evaluate the safety and efficacy of the Cutera truSculpt radiofrequency device for circumferential reduction.
Detailed description
The objectives of this study are to evaluate efficacy and safety of treatment with the Cutera truSculpt RF device for circumferential reduction in the abdominal and flank region.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | truSculpt rf device | radiofrequency device |
Timeline
- Start date
- 2016-03-01
- Primary completion
- 2016-09-01
- Completion
- 2016-09-01
- First posted
- 2016-08-19
- Last updated
- 2018-02-28
- Results posted
- 2018-02-28
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT02873104. Inclusion in this directory is not an endorsement.