At a glance
ClinicalIndex Comparison RecordN/ACompleted· 10 enrolled
Drug / intervention
MotifMESHdevice
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 Outcome Study of Condensed Fenestrated PTFE Mesh (MotifMESH) in Non-sterile Abdominal Wall Defects
In Brief
A clinical study evaluating MotifMESH for Hernia. Completed, enrolled 10 participants across 1 site.
Detailed Summary
This study will monitor surgically repaired large abdominal hernias requiring condensed fenestrated polytetrafluoroethylene mesh (cPTFE).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHernia
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
Enrollment StartMay 2011
First PostedJun 2011
Primary CompletionMar 2014
TodayJul 2026
First PostedJun 2, 2011
Enrollment StartMay 1, 2011
Primary CompletionMar 1, 2014
TodayJul 2, 2026
Enrollment to primary: 2.8 yearsPosted 15.1 years ago
Interventions
MotifMESHdevice
Polytetrafluoroethylene (cPTFE) macroporous mesh