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NCT04749095 Clinical Trial

Erector Spinae Plane Block Analgesia for Lumbar Spine Fusion Surgery

Pain, Postoperative Clinical Trial

Official title:
Can Bilateral Erector Spinae Plane Block Minimize Perioprative Opioid Consumption and Provide Satisfactory Analgesia for Lumbar Spine Fusion Surgery? A Randomized Controlled Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04749095
Other study ID # erector spinae plane block
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 2021
Est. completion date September 2021

Study information
Verified date February 2021
Source Benha University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 45
Est. completion date September 2021
Est. primary completion date August 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 65 Years
Eligibility 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

Related Conditions & MeSH terms

Intervention

Drug:
• Erector spinae plane block
bilateral ESP block will be injected with 20 ml of 0.25% bupivacaine
• sham subcutaneous infiltration
bilateral ESP block will be injected with 20 ml of normal saline

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Benha University

Outcome
Type Measure Description Time frame Safety issue
Primary Analgesia Numerical rating scale of pain every 6 hours Up to 24 hours after surgery
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