At a glance
ClinicalIndex Comparison RecordN/ACompleted· 33 enrolled
Drug / intervention
Resorbable Meshdevice
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, Multicenter All Comers Study of a Novel Resorbable Mesh (Phasix Mesh) for Ventral or Incisional Hernia Repair
In Brief
A clinical study evaluating Resorbable Mesh for Ventral Hernia and Incisional Hernia. Completed, enrolled 33 participants across 6 sites.
Detailed Summary
Collect data on safety, performance, and effectiveness of Phasix Mesh in subject requiring primary ventral and incisional hernias.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsVentral Hernia, Incisional Hernia
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
Enrollment StartFeb 2014
First PostedFeb 2014
Primary CompletionFeb 2017
TodayJul 2026
First PostedFeb 3, 2014
Enrollment StartFeb 1, 2014
Primary CompletionFeb 23, 2017
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 12.4 years ago
Interventions
Resorbable Meshdevice
Phasix Mesh