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

2014-08-27 03:13:54 | BioPortfolio

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.

Description

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

Study Design

Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment

Conditions

Postoperative Pain

Intervention

Placebo (one of medication), Ropivacaine (epidural injection)

Location

ChungAng University
Seoul
Korea, Republic of
156-755

Status

Not yet recruiting

Source

Chung-Ang Univerisity Hospital

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:13:54-0400

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