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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | suture | suture for mesh fixation |
| PROCEDURE | no suture | no 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.