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Clinical Trials/NCT05465967
NCT05465967
Unknown
Not Applicable

A Comparative Study Between Two Approaches of Ultrasound-Guided Transmuscular Quadratus Lumborum Block on Post-Operative Analgesia After Total Hip Arthroplasty

Tanta University1 site in 1 country75 target enrollmentSeptember 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Quadratus Lumborum Block
Sponsor
Tanta University
Enrollment
75
Locations
1
Primary Endpoint
Postoperative morphine consumption
Last Updated
3 years ago

Overview

Brief Summary

The aim of this study is to compare between the post-operative analgesic effect of two approaches of transmuscular quadratus lumborum block (transverse versus paraspinous sagittal transmuscular QLB) in total hip replacement surgery.

Detailed Description

During the preanesthetic assessment, all patients will be educated about the visual analogue scale (VAS) for pain assessment, with scores ranging from 0 to 10 (0 represent no pain, while10 represent maximum intolerable pain). The patients will be randomly classified into three equal groups (25 patients each). Group allocation will be done by computer generated random numbers and closed opaque sealed envelopes. The study will be designed to be double blind as all patients and postoperative assessor will be blinded to group assignment. Patients will be randomized to one of three equal groups: * Group I: Control group (n= 25 patients): Patients in this group will receive ipsilateral sham ultrasound-guided block via subcutaneous injection of 1 ml of normal saline after surgery. * Group II (n= 25 patients): Patients in this group will receive an ipsilateral single shot of transverse transmuscular approach of QLB (30 ml of plain bupivacaine 0.25%) after surgery using ultrasonographic guidance. * Group III (n= 25 patients): patients in this group will receive an ipsilateral single-shot of paraspinous sagittal approach of QLB (30 ml of plain bupivacaine 0.25%) after surgery using ultrasonographic guidance.

Registry
clinicaltrials.gov
Start Date
September 1, 2021
End Date
September 1, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mai Abdelhaleem Kamal Nida

assistant lecturer

Tanta University

Eligibility Criteria

Inclusion Criteria

  • 75 patients, aged between 21- 80 years old, of both sex American society of Anesthesiology I - III scheduled for total hip replacement surgery.

Exclusion Criteria

  • Patient refusal.
  • Coagulopathy
  • Spinal deformities
  • Peripheral neuropathy; sensory disorders in the leg requiring surgery and chronic pain.
  • Mental dysfunction, psychiatric illnesses and cognitive dysfunction.
  • History of drug abuse \&chronic analgesic use

Outcomes

Primary Outcomes

Postoperative morphine consumption

Time Frame: Baseline

Total Morphine consumption in the first 24 h of the post-operative period .

Secondary Outcomes

  • Postoperative pain score(Baseline)

Study Sites (1)

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