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Clinical Trial Summary

Randomized controlled trial on mesh fixation using cyanoacrylate glue compared to standard suture in open inguinal hernia repair.


Clinical Trial Description

Hernioplasty with suture-fixed mesh is the standard technique for the treatment of inguinal hernia, one of the most frequent pathologies in the Surgery Service. Despite its good results in terms of recurrences, it is currently under review due to the incidence of chronic postoperative pain. Up to half of the patients report some type of pain at one year of follow-up, and 15% report moderate-severe pain. The objective of the study is to analyze whether the use of tissue adhesive (n-hexyl cyanoacrylate 0.5 ml) for mesh fixation in patients undergoing scheduled open inguinal hernioplasty results in a better postoperative evolution, with less chronic pain and less demand for analgesia, compared with a control group of patients who undergo the same surgical intervention with standard suture repair. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05934266
Study type Interventional
Source Hospital Universitario de Móstoles
Contact Justyna Drewniak
Phone +34916648600
Email justyna.drewniak@salud.madrid.org
Status Recruiting
Phase Phase 4
Start date March 29, 2023
Completion date November 29, 2023

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