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
Investigators
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
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