Impact of Mesh Fixation With Tissue Adhesive

Status Recruiting

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

Clinical Trial Details

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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