CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 7 enrolled
Drug / intervention
TempSure treatmentdevice
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/NCT04881149
NCT04881149N/ACompleted
CompareCT.gov

Rollover Study to Evaluate Histological Results of Radiofrequency Device Treatments on the Flanks

Cynosure, Inc.·interventional·Posted May 11, 2021·Updated Jun 1, 2022

In Brief

A clinical study evaluating TempSure treatment for Skin Laxity. Completed, enrolled 7 participants across 1 site.

Detailed Summary

The purpose of this study is to evaluate histological results of the treatments with the TempSure Firm handpiece on the flanks performed in the CYN20-FIRM-LIPO study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSkin Laxity
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedMay 11, 2021
Enrollment StartFeb 12, 2021
Primary CompletionMar 10, 2021
TodayJul 2, 2026
Enrollment to primary: 28 daysPosted 5.1 years ago

Interventions

TempSure treatmentdevice

Self-controlled, single-arm study using the TempSure device.