Clinical Trials Directory

Trials / Completed

CompletedNCT00815698

Effect of Suture for Mesh Fixation in Lichtenstein Hernia Repair

Effect of Suture for Mesh Fixation in Lichtenstein Hernia Repair, a Prospective Controlled Randomized Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
334 (actual)
Sponsor
Jacob Rosenberg · Academic / Other
Sex
Male
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The investigators want to evaluate the effect of suturing the mesh versus using a self-adhesive mesh for Lichtenstein hernia repair. Effect parameters include chronic pain.

Detailed description

Pain is a frequent problem after open inguinal hernia repair. The most frequent operative technique for inguinal hernia repair in adults is the Lichtenstein mesh repair, where a polypropylene mesh is sutured to the tissue in the inguinal region. We therefore want to evaluate the effect of suture for mesh fixation on the occurrence of chronic pain 12 months after operation.

Conditions

Interventions

TypeNameDescription
PROCEDUREsuturesuture for mesh fixation
PROCEDUREno sutureno suture for mesh fixation, because we use a self-adhesive mesh

Timeline

Start date
2008-12-01
Primary completion
2011-04-01
Completion
2011-09-01
First posted
2008-12-30
Last updated
2016-03-23
Results posted
2016-03-23

Locations

5 sites across 1 country: Denmark

Source: ClinicalTrials.gov record NCT00815698. Inclusion in this directory is not an endorsement.