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Clinical Trials/NCT04749095
NCT04749095
Unknown
Not Applicable

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

Benha University0 sites45 target enrollmentMay 2021
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ConditionsPain, Postoperative
InterventionsErector spinae plane blocksham subcutaneous infiltration
DrugsErector spinae plane blocksham subcutaneous infiltration

Overview

Phase
Not Applicable
Intervention
Erector spinae plane block
Conditions
Pain, Postoperative
Sponsor
Benha University
Enrollment
45
Primary Endpoint
Analgesia
Last Updated
5 years ago
OverviewInvestigatorsEligibility CriteriaArms & InterventionsOutcomesSimilar Trials

Overview

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.

Registry
clinicaltrials.gov
Start Date
May 2021
End Date
September 2021
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Baher Said Elshahat Mohamed Abdelhady

Principal Investigator

Benha University

Eligibility Criteria

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

Arms & Interventions

Erector block

Intervention: Erector spinae plane block

sham block

Intervention: sham subcutaneous infiltration

Outcomes

Primary Outcomes

Analgesia

Time Frame: Up to 24 hours after surgery

Numerical rating scale of pain every 6 hours

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