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Clinical Trials/NCT05247021
NCT05247021
Unknown
Phase 4

Bilateral Ultrasound Guided Erector Spinae Plane Block for Postoperative Pain Management in Lumbar Spine Surgery ( a Controlled Study Trial)

Ain Shams University1 site in 1 country44 target enrollmentJanuary 22, 2021
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ConditionsLumbar Disc Disease

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Lumbar Disc Disease
Sponsor
Ain Shams University
Enrollment
44
Locations
1
Primary Endpoint
the postoperative 24 hours morphine consumption
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

Aim of this study was to assess the efficacy of erector spinae plane block (ESB) for postoperative pain management in lumbar spine surgery.

Registry
clinicaltrials.gov
Start Date
January 22, 2021
End Date
June 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •Patients American Society of Anesthesiologists physical status (ASA) I and II.
  • •Both sexes.
  • •Age between 20 to 60 years old.
  • •Scheduled for lumbar spine surgeries.

Exclusion Criteria

  • •Patients who received long acting opioids preoperatively.
  • •Patients with bleeding disorders and coagulopathy.
  • •Infection at the injection site.
  • •Allergy to local anesthetics.
  • •Patients with significant cognitive dysfunction.
  • •Patients with diabetic neuropathy.
  • •Patients with uncontrolled hypertension or diabetes.
  • •Patients with advanced cardiac, respiratory, hepatic or renal disease.
  • •Patients with viral hepatitis or HIV.

Outcomes

Primary Outcomes

the postoperative 24 hours morphine consumption

Time Frame: 24 hours postoperative

the analgesic effect of erector spine block will be assessed postoperative by numeric rating scale (NRS), if NRS is more than 3 the patient will receive a rescue dose of 5 milligrams of morphine

Secondary Outcomes

  • Mean Blood pressure in mmHg(24 hours postoperative)
  • First time of mobilization to a chair(24 hours postoperative)
  • Patient satisfaction(24 hours postoperative)
  • Heart rate(24 hours postoperative)

Study Sites (1)

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