Laparoscopic Hernia Defect Obliteration With ProFlor-E

Status Completed

Clinical Trial Summary

This feasibility study highlights the features of the 3D dynamic responsive prosthesis ProFlor-E® for fixation free obliteration of inguinal hernia defect

Clinical Trial Description

The 3D dynamic-responsive prosthesis for inguinal hernia repair ProFlor-E® recently introduced to the market has been laparoscopically employed for the repair of one recurrent inguinal hernia previously managed with anterior open approach. The scope of this feasibility study is to demonstrate that the positive effects of the 3D implant already proven in open inguinal hernia repair are also effective or even superior for the laparoscopic of recurrent/bilateral inguinal hernias compared to conventional treatment concept. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04718298
Study type	Interventional
Source	University of Cagliari
Contact
Status	Completed
Phase	N/A
Start date	June 1, 2019
Completion date	June 1, 2021

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See also
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