At a glance
ClinicalIndex Comparison RecordN/ACompleted· 35 enrolled
Drug / intervention
Flex HD +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.
Feasibility Study of The Use of FLEX HD® Surgical Implant or STRATTICE® Reconstructive Tissue Matrix in The Closure of Abdominal Wall Defects With Component Separation in Clean or Contaminated Cases
In Brief
A clinical study evaluating Flex HD and Strattice for Hernia Repair With Compartment Syndrome. Completed, enrolled 35 participants across 1 site.
Detailed Summary
This study examines the feasibility of using Flex HD® Surgical Implant or STRATTICE® Reconstructive Tissue Matrixin the repair of hernias.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHernia Repair With Compartment Syndrome
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
Enrollment StartMar 2011
First PostedMay 2012
Primary CompletionMay 2015
TodayJul 2026
First PostedMay 11, 2012
Enrollment StartMar 1, 2011
Primary CompletionMay 1, 2015
TodayJul 2, 2026
Enrollment to primary: 4.2 yearsPosted 14.1 years ago
Interventions
Flex HDdevice
Flex HD mesh for hernia repair
Stratticedevice
Strattice mesh for hernia repair