CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 37 enrolled
Drug / intervention
Ulthera® Systemdevice
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/NCT01713933
NCT01713933N/ACompleted

Evaluation of the Ulthera® System for Obtaining Lift and Tightening of the Brachia

Ulthera, Inc·interventional·Posted Oct 25, 2012·Updated Dec 11, 2017

In Brief

A clinical study evaluating Ulthera® System for Brachial Ptosis. Completed, enrolled 37 participants across 1 site.

Detailed Summary

This study is an evaluation of the Ulthera® System used to treat the upper arms for improvement of brachial ptosis. All enrolled subjects will receive one bilateral upper arm treatment. Follow-up visits will occur at 60, 90 and 180 days post-treatment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsBrachial Ptosis
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedOct 25, 2012
Enrollment StartJun 1, 2011
Primary CompletionFeb 1, 2012
Study CompletionMay 1, 2012
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 13.7 years ago

Interventions

Ulthera® Systemdevice

Focused ultrasound energy delivered below the surface of the skin.