Postoperative analgesic efficacy of erector spinae plane block for lumbar spinal surgery

Phase 2

Completed

• Conditions: lumbar spine surgery; erector spinae plane block; postoperative morphine consumption; postoperative pain

• Registration Number: TCTR20190311002
• Lead Sponsor: Faculty of medicine, Khon Kaen University, Thailand

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-03-11
• Study Completion: 2020-03-30
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 62

Inclusion Criteria

age 18-75 years
ASA physical status 1-3
understand and can operate the IV PCA device

Exclusion Criteria

previous lumbar spine surgery
allergy to study drugs
chronic used of opioids
coagulopathy

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Morphine consumption 0,6,12, 24,48 hour, postoperatively data from IV PCA device

Secondary Outcome Measures

Name	Time	Method
postoperative pain score 0,6,12, 24,48 hour, postoperatively self reported numeric rating pain score