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SEMPERFLO* Pain Management System in Inguinal Hernia Repair

Pain Clinical Trial

Official title:
A Prospective, Randomized, Exploratory Comparison of the SEMPERFLO* Pain Management System to a Commercially Available Pain Relief System in Subjects Undergoing Open Inguinal Hernia Repair

Clinical Trial Summary

This study will compare the clinical performance of the SEMPERFLO* Pain Management System with another commercial pain relief system using 0.5% bupivacaine following unilateral, open, inguinal hernia repair procedures.

*Trademark

Clinical Trial Description

Pain will be evaluated up to 5 days after surgery Subjects will be followed for 30 days after surgery. ;

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00423241
Study type Interventional
Source Ethicon, Inc.
Contact
Status Terminated
Phase N/A
Start date January 2007
Completion date January 2008
View Details
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