At a glance
ClinicalIndex Comparison RecordN/ACompleted· 55 enrolled
Drug / intervention
Subcutaneous tissue release with the Cabochon 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.
Pivotal Study of the Cabochon System for Improvement in the Appearance of Cellulite
In Brief
A clinical study evaluating Subcutaneous tissue release with the Cabochon System for Gynoid Lipodystrophy. Completed, enrolled 55 participants across 3 sites.
Detailed Summary
The purpose of this study is to evaluate the safety and effectiveness of the Cabochon System for the improvement in the appearance of cellulite.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsGynoid Lipodystrophy
CountriesUnited States
CollaboratorsUlthera, Inc
Timeline
N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
Enrollment StartAug 2012
First PostedAug 2012
Primary CompletionSep 2013
Study CompletionDec 2015
TodayJul 2026
First PostedAug 24, 2012
Enrollment StartAug 1, 2012
Primary CompletionSep 1, 2013
Study CompletionDec 1, 2015
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 13.9 years ago
Interventions
Subcutaneous tissue release with the Cabochon Systemdevice
Device: Subcutaneous tissue release