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Quadratus Lumborum Block Using Loss-of-resistance Versus Ultrasound-guided Technique

Not Applicable
Conditions
Quadratus Lumborum Block
Lower Abdominal Surgery
Interventions
Procedure: Ultrasound-guided Quadratus lumborum block
Procedure: Loss-of-resistance Quadratus lumborum block
Procedure: General anesthesia
Registration Number
NCT03328481
Lead Sponsor
Cairo University
Brief Summary

This study aims to explore the feasibility of using loss-of-resistance technique for Quadratus Lumborum block (QLB). And to compare between the Ultrasound guided QLB type II and the loss-of-resistance technique for QLB as regards the degree and duration of analgesia and side effects.

Detailed Description

Quadratus lumborum block (QLB) is an abdominal plane block with increasing popularity. QLB is achieved by local anesthetic infiltration at the anterolateral aspect of quadratus lumborum muscle (QLB-I), or at the posterior aspect of the muscle (QLB-II), or transmuscular (QL-TM block). Ultrasound-guided technique is the usual route used for QLB performance. QLB had been considered a modification of transversus abdominis plane (TAP) block\[4\]. A cadaveric study had showed similar local anesthetic spread in both QL and TAP blocks.

TAP block could be performed by using either the ultrasound or loss-of-resistance technique; whilst, QLB is only performed using the ultrasound and the feasibility of loss-of-resistance technique had not been investigated for this block.

This study aims to explore the feasibility of using loss-of-resistance technique for QLB. And to compare between the Ultrasound guided QLB type II and the loss-of-resistance technique for QLB as regards the degree and duration of analgesia and side effects.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
16
Inclusion Criteria
  • Patients scheduled for lower abdominal surgery under general anesthesia
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Exclusion Criteria
  • Patient refusal to regional block,
  • Pregnancy
  • Coagulopathy
  • Cognitive impairment
  • Inflammation or infection at the puncture site
  • History of allergic reaction to study medications
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Loss-of-resistanceGeneral anesthesiaPatients in this group will receive Loss-of-resistance Quadratus lumborum block with 30 ml bupivacaine 0.25% in addition to general anesthesia.
Ultrasound-guidedUltrasound-guided Quadratus lumborum blockPatients in this group will receive Ultrasound-guided Quadratus lumborum block type-II with 30 ml bupivacaine 0.25% in addition to general anesthesia.
Loss-of-resistanceLoss-of-resistance Quadratus lumborum blockPatients in this group will receive Loss-of-resistance Quadratus lumborum block with 30 ml bupivacaine 0.25% in addition to general anesthesia.
Ultrasound-guidedGeneral anesthesiaPatients in this group will receive Ultrasound-guided Quadratus lumborum block type-II with 30 ml bupivacaine 0.25% in addition to general anesthesia.
Primary Outcome Measures
NameTimeMethod
Duration of analgesia24 hours

The time between the end of the surgery and the first analgesia request

Secondary Outcome Measures
NameTimeMethod
Postoperative morphine consumption24 hours

The total amount of morphine needed during the first 24 hours

Intraoperative extra-analgesia requirements3 hours

The total amount of analgesic drug boluses

visual analogue pain score at rest to assess the pain severity24 hours

the grade of pain experienced by the patient at rest graded from 0 to 10. The lower the value, the better the score

Visual analogue pain score at movement to assess the pain severity24 hours

the grade of pain experienced by the patient at movement graded from 0 to 10. The lower the value, the better the score

Systolic blood pressure24 hours

the systolic blood pressure measured in mmHg

Heart rate24 hours

The number of heart beats per minute

Trial Locations

Locations (1)

Cairo University

🇪🇬

Cairo, Egypt

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