Skip to main content
Clinical Trials/NL-OMON25668
NL-OMON25668
Not yet recruiting
Not Applicable

A double-blind randomized controlled trial comparing the effect of using Parietene self-fixing semi-Resorbable mesh with standard heavy-weight polypropylene mesh on inguinal pain development following inguinal herniorrhaphy

MJA Loos MDDepartment of SurgeryMaxima Medical CentreDe Run 4600, 5500 MB Veldhoven, the Netherlands0 sites350 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Inguinal hernia, mesh, chronic painHernia inguinalis, mesh, chronische pijn
Sponsor
MJA Loos MDDepartment of SurgeryMaxima Medical CentreDe Run 4600, 5500 MB Veldhoven, the Netherlands
Enrollment
350
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

/A

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
MJA Loos MDDepartment of SurgeryMaxima Medical CentreDe Run 4600, 5500 MB Veldhoven, the Netherlands

Eligibility Criteria

Inclusion Criteria

  • 1\. Age 18 years or older
  • 2\. Unilateral primary inguinal hernia

Exclusion Criteria

  • 1\. Incarcerated inguinal hernia
  • 2\. Local inguinal inflammation

Outcomes

Primary Outcomes

Not specified

Similar Trials