Trials / Completed
CompletedNCT05254210
Feasibility Study To Collect Safety And Preliminary Efficacy Data For A Radiofrequency Microneedling Device
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 10 (actual)
- Sponsor
- Cynosure, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
The intended use of the Potenza™ device is to collect clinical data for brow lifting and/or treatment of dermatologic conditions in which electrocoagulation and hemostasis is a viable mechanism for means of improvement.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | RF Device (Potenza™) | Test spots may be performed prior to the first treatment. Following test spots, for the treatment, the tip will be placed in contact with the skin. Parameters may be adjusted throughout the treatment and will determined by the Clinician. |
Timeline
- Start date
- 2021-09-13
- Primary completion
- 2022-05-17
- Completion
- 2022-05-17
- First posted
- 2022-02-24
- Last updated
- 2023-08-15
- Results posted
- 2023-08-15
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05254210. Inclusion in this directory is not an endorsement.