Erector Spinae Plane Block Analgesia for Lumbar Spine Fusion Surgery

Not Applicable

• Conditions: Pain, Postoperative
• Interventions: Drug: Erector spinae plane block; Drug: sham subcutaneous infiltration

• Registration Number: NCT04749095
• Lead Sponsor: Benha University

Brief Summary

The purpose of this study was to investigate the effect of a bilateral ultrasound guided erector spinae plane block on the pain scores and opoid utiliziation in fusion surgery of the lumbar spine.

Detailed Description

Not available

Study Timeline

• Status Verified: 2021-02
• Study First Submitted: 2021-02-05
• Study First Submitted QC: 2021-02-09
• Last Update Submitted: 2021-02-09
• Study First Posted: 2021-02-11
• Last Update Posted: 2021-02-11
• Study Start: 2021-05
• Primary Completion: 2021-08
• Study Completion: 2021-09

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 45

Inclusion Criteria

• American Society of Anesthesiologists class I-III adult patients
• BMI less than or equal 35 kg/m2

Exclusion Criteria

• Patient refusal
• unable to give consent
• age < 18 or > 65
• BMI more than 35 kg/m2
• known allergy to the study medication
• coagulopathies or on anticoagulant medications
• hepatic insufficiency
• renal insufficiency
• chronic opioid use

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Erector block	Erector spinae plane block	-
sham block	sham subcutaneous infiltration	-

Primary Outcome Measures

Name	Time	Method
Analgesia	Up to 24 hours after surgery	Numerical rating scale of pain every 6 hours