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Clinical Trials/NCT04757480
NCT04757480UnknownNot Applicable

Ultrasound Guided Thoracolumbar Interfascial Plane Block Versus Bilateral Ultrasound Guided Erector Spinae Plane Block for Post-Operative Pain Management In Lumbar Laminectomy

Tanta University2 sites in 1 country70 target enrollmentStarted: March 1, 2021Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
70
Locations
2
Primary Endpoint
Degree of pain by visual Analog Scale (VAS) score at rest
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The aim of this prospective randomized trial is to compare the efficacy ultrasound guided thoracolumbar interfascial plane block versus bilateral ultrasound guided erector spinae plane block for post-operative pain management after lumbar laminectomy

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
21 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Seventy cases with herniated lumbar disc scheduled for lumbar single-level or multiple-level lumbar discectomy with American Society of Anesthesiologists physical status (ASA) I or II aged between 21 and 60 years of both genders.

Exclusion Criteria

  • •Body mass index >32
  • •History of relevant allergy to any of the drugs used in the procedure
  • •Previous lumbar spine surgery or back surgery with planed spinal fixation

Outcomes

Primary Outcomes

Degree of pain by visual Analog Scale (VAS) score at rest

Time Frame: First 24 hours postoperative

Pain scores will be observed and recorded using the Visual Analog Scale (VAS) both at rest and during movement. The scores will be recorded in the ward at 2, 4, 8, 12, and 24 h. VAS score from 0 to 10 (0: No pain, 10: The worst pain)

Secondary Outcomes

  • Degree of pain by visual Analog Scale (VAS) score at movement(First 24 hours postoperative)
  • 24-h morphine consumption(First 24 hours postoperative)
  • Total rescue analgesics consumption(First 24 hours postoperative)
  • The time to first analgesic(First 24 hours postoperative)
  • Side effects associated with morphine(First 24 hours postoperative)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Aliaa Mohammad Abdel Reeheem Abdel kader

Assistant lecturer of Anesthesiology, Surgical Intensive Care and Pain Medicine

Tanta University

Study Sites (2)

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