At a glance
ClinicalIndex Comparison RecordN/ACompleted· 10 enrolled
Drug / intervention
RF Device (Potenza™)device
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Feasibility Study To Collect Safety And Preliminary Efficacy Data For A Radiofrequency Microneedling Device
In Brief
A clinical study evaluating RF Device (Potenza™) for Wrinkles and 6 related conditions. Completed, enrolled 10 participants across 1 site.
Detailed 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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsWrinkles, Fine Lines, Crepey Skin, Acne Scars, Active Acne, Enlarged Pores, Loose Skin
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20222023202420252026
Enrollment StartSep 2021
First PostedFeb 2022
Primary CompletionMay 2022
TodayJul 2026
First PostedFeb 24, 2022
Enrollment StartSep 13, 2021
Primary CompletionMay 17, 2022
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 4.4 years ago
Interventions
RF Device (Potenza™)device
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.