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Trigger-point Blockade in Persistent Pain After Laparoscopical Groin Hernia Repair — Trigger-lap  

Chronic Pain Clinical Trial

Official title:
Trigger-point Blockade in Persistent Pain After Laparoscopically Assisted Groin Hernia Repair

Clinical Trial Summary

Groin hernia repair is a common procedure performed in approximately 2,000 patients per one million inhabitants. Severe chronic pain following groin hernia repair is seen in 2-5% of the patients indicating that a large number of patients each year suffer from debilitating reduction in health-related quality of life.

This study examines the effect of ultra-sound guided blocks with local anesthesia in the groin in regard to pain relief and sleep quality.

The hypothesis of the study is that a block will confer significant pain relief to patients with severe chronic pain following laparoscopical groin hernia repair.

Clinical Trial Description

This placebo-controlled, randomized, double-blind, cross-over study in subjects with severe pain after laparoscopically assisted groin hernia repair, examines the effect of an ultra-sound guided local anesthetic block of a trigger-point, situated near the spermatic cord at the superficial inguinal ring. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02065804
Study type Interventional
Source University of Copenhagen
Contact
Status Completed
Phase Phase 3
Start date October 2013
Completion date July 2014
View Details
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