Erector spina block in lumbar spinal surgery

Phase 3

Recruiting

• Conditions: Pain control after spinal surgery.; Other acute postprocedural pain; G89.18

• Registration Number: IRCT20200628047936N1
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 October 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

All candidated 18-75 y/o patients for spinal lumbar surgery
patients with normal hepatic and renal function
ASA score 1-2

Exclusion Criteria

addiction
BMI more than 35 or less than 16
allergy to local anesthetics
mental disorders

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postop pain score in defined intervals. Timepoint: 1, 2 , 4, 6, 12, 24 Hours after surgery. Method of measurement: Pain scale chart (NRS).;Opioid consumption in first postop 24 hours. Timepoint: First 24 hours. Method of measurement: Amount of Opioid consumption recorded by nurse.