At a glance
ClinicalIndex Comparison RecordN/ACompleted· 100 enrolled
Drug / intervention
Not specified
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.
Observational Registry Study for Symbotex™ Composite Mesh in Ventral Hernia Repair
In Brief
An observational study for Ventral Incisional Hernia. Completed, enrolled 100 participants across 1 site.
Detailed Summary
The aim of this Observational Registry Study is to assess the short- and long-term clinical outcomes following the use of Symbotex™ Composite Mesh in primary and incisional abdominal wall hernia surgeries by open or laparoscopic approach, according to the Instruction for use (IFU).
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsVentral Incisional Hernia
CountriesFrance
Collaborators--
Timeline
N/ACompletedFinished
201520162017201820192020202120222023202420252026
Enrollment StartJun 2014
First PostedAug 2014
Primary CompletionMay 2017
TodayJul 2026
First PostedAug 1, 2014
Enrollment StartJun 25, 2014
Primary CompletionMay 22, 2017
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 11.9 years ago