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A Preemptive Epidural Ropivacaine for Postoperative Pain Relief in Degenerative Lumbar Spine Surgery

Postoperative Pain Clinical Trial

Official title:
A Preemptive Epidural Ropivacaine for Postoperative Pain Relief in Degenerative Lumbar Spine Surgery: A Prospective Randomized Study

Clinical Trial Summary

This prospective randomized study aims to evaluate the effectiveness of epidural injection of ropivacaine on the relief of pain in patients undergoing laminectomy.

Total 60 patients will be randomized into one of two groups (groupC or groupI) based on Excel number generation.

Patients in group C will receive no medication intraoperatively, and patients in group I will receive epidural injection of 0.1% ropivacaine 10ml before skin incision.

Visual analogue scale pain scores, fentanyl consumption and the frequency at which patients pushed the button (FPB) of a patient-controlled analgesia system will be recorded at 4,12,24,48 hour postoperatively.

Clinical Trial Description

Patients in group I will receive 0.1% ropivacaine 10 ml before skin incision under guide of C-arm. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01117610
Study type Interventional
Source Chung-Ang University Hosptial, Chung-Ang University College of Medicine
Contact
Status Unknown status
Phase Phase 4
Start date May 2010
Completion date April 2011
View Details
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