At a glance
ClinicalIndex Comparison RecordN/ACompleted· 15 enrolled
Drug / intervention
ProFlor Hernia implantdevice
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.
Neo-neurogenesis in 3D Dynamic Responsive Implant for Inguinal Hernia Repair PorFlor
In Brief
A clinical study evaluating ProFlor Hernia implant for Inguinal Hernia. Completed, enrolled 15 participants.
Detailed Summary
The investigation is aimed at specifically demonstrating the ingrowth of newly formed nervous elements within a 3D dynamic responsive implant for inguinal hernia repair.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsInguinal Hernia
Countries--
Collaborators--
Timeline
N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
Enrollment StartJan 2013
Primary CompletionDec 2016
First PostedNov 2019
TodayJul 2026
First PostedNov 20, 2019
Enrollment StartJan 1, 2013
Primary CompletionDec 1, 2016
TodayJul 2, 2026
Enrollment to primary: 3.9 yearsPosted 6.6 years ago
Interventions
ProFlor Hernia implantdevice
Inguinal hernia repair