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Parastomal Reinforcement With Strattice — PriSm  

Parastomal Hernia Clinical Trial

Official title:
A Prospective, Multicenter, Randomized, Controlled, Third-party Blinded Study of Strattice Fascial Inlay for Parastomal Reinforcement in Patients Undergoing Surgery for Permanent Abdominal Wall Ostomies

Clinical Trial Summary

The purpose of this study is to compare the clinical outcomes of patients undergoing surgery for a permanent abdominal wall ostomy with and without placement of Strattice fascial inlay, as measured by postoperative occurence of parastomal hernia.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Outcomes Assessor)

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00771407
Study type Interventional
Source LifeCell
Contact
Status Completed
Phase Phase 4
Start date December 2008
Completion date July 2012
View Details
See also
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