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Transversus Abdominis Plane Block and Inguinal Hernia Repair

Postoperative Pain Clinical Trial

Official title:
The Analgesic Efficacy of the Ultrasound Guided Transversus Abdominis Plane Block After Inguinal Hernia Repair With a Mesh.

Clinical Trial Summary

This prospective, randomized, double blinded, placebo-controlled study is designed to evaluate the postoperative analgesic efficacy of the ultrasound-guided transversus abdominis plane block with ropivacaine 0,75 %, in patients undergoing unilateral inguinal hernia repair with a mesh under general anaesthesia, and how the efficiency of early postoperative analgesia achieved correlates with the risk of developing a chronic pain state, a not uncommon condition after this type of surgery.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02030223
Study type Interventional
Source Aretaieion University Hospital
Contact
Status Completed
Phase N/A
Start date January 2014
Completion date December 2017
View Details
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