Intraperitoneal Mesh-Implementation After Laparotomy

Status Active, not recruiting

Clinical Trial Summary

Aim of the study is to evaluate the risk reduction of intraperitoneal mesh-implementation after laparotomy (Group 1) in a randomized control trial compared with patients with standard abdominal closure (Everett-suture). This is the primary endpoint. Second endpoints are the feasibility of mesh-implementation even after colorectal surgery, find risk factors for wound infection and incisional hernia.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01003067
Study type	Interventional
Source	Kantonsspital Liestal
Contact
Status	Active, not recruiting
Phase	N/A
Start date	March 2008
Completion date	June 2020

View Details

See also
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