At a glance
ClinicalIndex Comparison RecordN/ACompleted· 229 enrolled
Drug / intervention
V-Loc 180/90 Wound Closure Device +1 moredevice
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.
A Prospective, Randomized Study to Evaluate Dermal Closure With an Absorbable Barbed Suture (V-Loc 180 Absorbable Wound Closure Device or V-Loc 90 Absorbable Wound Closure Device) as Compared to a Conventional Absorbable Suture
In Brief
A clinical study evaluating V-Loc 180/90 Wound Closure Device and 3-0 Monocryl Absorbable Sutures for Breast Ptosis and Obesity. Completed, enrolled 229 participants across 8 sites in 2 countries.
Detailed Summary
The objective of this study is to evaluate the use of an absorbable barbed suture as compared to a conventional absorbable suture when used for dermal closure during certain body contouring procedures.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsBreast Ptosis, Obesity
CountriesGermany, United States
Collaborators--
Timeline
N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
Enrollment StartAug 2009
First PostedAug 2009
Primary CompletionMay 2011
Study CompletionFeb 2012
TodayJul 2026
First PostedAug 14, 2009
Enrollment StartAug 1, 2009
Primary CompletionMay 1, 2011
Study CompletionFeb 1, 2012
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 16.9 years ago
Interventions
V-Loc 180/90 Wound Closure Devicedevice
Barbed absorbable suture
3-0 Monocryl Absorbable Suturesdevice
3-0 Monocryl Absorbable Suture (non-barbed)