Biological implants for the reconstruction of complex, contaminated abdominal wall defects.

Recruiting

• Registration Number: NL-OMON24625

Brief Summary

/A

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 80

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

N/A

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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.