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Progrip Versus ProFlor: Two Fixation Free Devices for Laparoscopic Inguinal Hernia Repair: A Randomized Clinical Trial: The ProPro Study
there are currently two methods for fixation free laparoscopic inguinal hernia repair specifically based on the intrinsic properties of the device used. The Progrip mesh technique leaves the hernia orifice patent and relies on the established principle of strengthening the groin through scar tissue incorporation induced by foreign body reaction. In contrast, the ProFlor concept introduces a 3D dynamic regenerative scaffold that permanently obliterates the defect and regenerates the herniated inguinal barrier. This report presents the outcomes of laparoscopic techniques employing Progrip and ProFlor in randomized clinical trial. The results of this clinical study may have the potential to pave the way for innovative advancements in hernia repair techniques.
Age
18 - 85 years
Sex
MALE
Healthy Volunteers
No
Italy
Palermo, Italy
Start Date
January 1, 2021
Primary Completion Date
December 31, 2023
Completion Date
December 31, 2025
Last Updated
August 16, 2024
150
ESTIMATED participants
Proflor group
PROCEDURE
Progrip group
PROCEDURE
Lead Sponsor
University of Palermo
NCT06879912
NCT07427043
Data Source & Attribution
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