Thoracolumbar Interfascial Plane Block Versus Bilateral Erector Spinae Plane Block In Lumbar Laminectomy

Not Applicable

• Conditions: Thoracolumbar Interfascial Plane Block; Erector Spinae Plane Block; Postoperative Pain; Ultrasound; Lumbar Laminectomy
• Interventions: Procedure: Thoracolumbar Interfascial Plane Block (TLIP); Procedure: Bilateral Erector Spinae plane Block (ESB)

• Registration Number: NCT04757480
• Lead Sponsor: Tanta University

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

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Status Verified: 2021-02
• Study First Submitted: 2021-02-14
• Study First Submitted QC: 2021-02-14
• Last Update Submitted: 2021-02-14
• Study First Posted: 2021-02-17
• Last Update Posted: 2021-02-17
• Study Start: 2021-03-01
• Primary Completion: 2021-09-30
• Study Completion: 2021-10-10

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 70

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.

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Exclusion Criteria

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

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Thoracolumbar Interfascial Plane Block (TLIP)	Thoracolumbar Interfascial Plane Block (TLIP)	-
Bilateral Erector Spinae plane Block (ESB)	Bilateral Erector Spinae plane Block (ESB)	-

Primary Outcome Measures

Name	Time	Method
Degree of pain by visual Analog Scale (VAS) score at rest	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 Outcome Measures

Name	Time	Method
Degree of pain by visual Analog Scale (VAS) score at movement	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)
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

Trial Locations

Locations (1)

Tanta University Hospitals; 🇪🇬 Tanta, ElGharbiaa, Egypt