None listed
Conditions
Interventions
None listed
Sponsors
None listed
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients with complex, contaminated wall defects, repaired with a biological mesh; 2. Patients with complex, contaminated wall defects, repaired with a synthetic mesh.
Exclusion criteria
Exclusion criteria: N/A
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome measure is the possible advantage of a biological mesh compared to the synthetic mesh, expressed in recurrence, morbidity, durability of the mesh (measured in the time passed postoperatively) and postoperative complications (measured in sepsis, reoperation and fistulation). | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome measure is the cost analysis of the biological mesh compared to the synthetic mesh determined in comparison with the case-matched control group. | — |
Contacts
Public ContactTina Loon, van
Surgery Department Atrium Medisch Centrum, Heerlen Henri Dunantstraat 5
Outcome results
None listed