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Prospective Clinical Observational Cohort Study to Evaluate the Use of a Tissue Separating Mesh (Proceed®) in Laparoscopic Ventral Hernia Repair

Ventral Hernia Clinical Trial

Official title:
Prospective Clinical Observational Cohort Study to Evaluate the Use of a Tissue Separating Mesh (Proceed®) in Laparoscopic Ventral Hernia Repair

Clinical Trial Summary

1. General: antibiotic prophylaxis: cefazoline (Cefacidal™) 2 gram iv administered 30 minutes before surgery 2. Laparoscopic surgery - at least 5 cm overlap (mesh diameter should exceed hernia size by at least 10 cm) - with or without anchoring transparietal sutures or double crown technique

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00572962
Study type Interventional
Source University Hospital, Ghent
Contact
Status Completed
Phase N/A
Start date January 2008
Completion date August 2014
View Details
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