Trials / Completed
CompletedNCT03018587
Feasibility Study of the TruSculpt Radiofrequency Device
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 23 (actual)
- Sponsor
- Cutera Inc. · Industry
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Accepted
Summary
A single-center, prospective, open-label feasibility study of the truSculpt radiofrequency device.
Detailed description
A single-center, prospective, open-label study to evaluate the safety and efficacy of the Cutera truSculpt radiofrequency device for optimal delivery of thermal energy to the skin.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | TruSculpt | All subjects will receive 1 truSculpt radiofrequency treatment |
Timeline
- Start date
- 2017-01-01
- Primary completion
- 2017-12-01
- Completion
- 2017-12-29
- First posted
- 2017-01-12
- Last updated
- 2023-03-07
- Results posted
- 2023-03-07
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03018587. Inclusion in this directory is not an endorsement.