CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 25 enrolled
Drug / intervention
Venus Vivadevice
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.

Search/NCT03776461
NCT03776461N/ACompleted

Clinical Evaluation of the Safety and Performance of Fractional Radiofrequency for the Treatment and Reduction of Facial Wrinkles

Venus Concept·interventional·Posted Dec 14, 2018·Updated Aug 15, 2023

In Brief

A clinical study evaluating Venus Viva for Rhytides and Wrinkle. Completed, enrolled 25 participants across 1 site.

Detailed Summary

Prospective, single centre, evaluator-blind study of the safety and performance of fractional radiofrequency (RF) for the treatment and reduction of facial wrinkles.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRhytides, Wrinkle
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedDec 14, 2018
Enrollment StartMar 8, 2019
Primary CompletionJun 18, 2021
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 7.5 years ago

Interventions

Venus Vivadevice

The Venus Viva™ is a non-invasive medical aesthetic device, intended for use in dermatologic and general surgical procedures, requiring ablation and resurfacing of the skin, using the Viva applicator.