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The Flemish Umbilical Nitinol Mesh Trial, a Multicenter Trial — FUN  

Umbilical Hernia Clinical Trial

Official title:
The Flemish Umbilical Nitinol Mesh Trial, a Multicenter Randomized Controlled Trial.

Clinical Trial Summary

The use of mesh in the repair of umbilical hernias is a gold standard. The best location of the mesh remains a matter of discussion, i.e. it might be placed inside the peritoneal cavity (open intraperitoneal onlay mesh) or between the peritoneum and the muscle layers, so not in contact with the viscera (retromuscular or preperitoneal). The Rebound mesh consists of polypropylene, i.e. the most used fabric for meshes, in combination with a nitinol memory ring. This ring allows the surgeon to position the mesh more flat, with less wrinkling and subsequently better tissue ingrowth. It also saves time for both patient's anesthesia and the surgery. This type of mesh (one coated with PTFE for intra-abdominal use and one pure polypropylene for preperitoneal use), will be used in this multicentric trial, to evaluate the best procedure in terms of efficacy, safety and postoperative complications.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01543789
Study type Interventional
Source University Hospital, Ghent
Contact
Status Completed
Phase N/A
Start date March 2012
Completion date December 31, 2023
View Details
See also
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