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A Prospective, Observational Study Utilizing Phasix™ Mesh During Ventral and Incisional Hernia Repair Surgery

Ventral Hernia Clinical Trial

Official title:
A Prospective, Observational Study Utilizing Phasix™ Mesh During Ventral and Incisional Hernia Repair Surgery

Clinical Trial Summary

The objective of this study is to collect efficacy, safety and utility data with Phasix™ Mesh in ventral and incisional repair procedures by evaluating the following:

1. Hernia recurrence rate of ventral and incisional hernias post repair with Phasix™ Mesh for up to 12 months post surgery.

2. Perioperative, short-term and long-term procedural and/or device related complications.

3. Abdominal Wall Function and mobility.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01863030
Study type Observational
Source University of Kentucky
Contact
Status Completed
Phase
Start date May 2013
Completion date November 2016
View Details
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