MedPath

ESPB vs PVB vs QLB After Pelvi-ureteric Surgeries

Not Applicable
Completed
Conditions
Analgesia
Quadratus Lumborum Block
Erector Spinae Plane Block
Paravertebral Block
Interventions
Procedure: ESPB Technique
Procedure: QLB Technique
Procedure: TPVB Technique
Registration Number
NCT05713643
Lead Sponsor
Kafrelsheikh University
Brief Summary

The aim of this study is to compare the analgesic efficacy of erector spinae plane block versus thoracic paravertebral block versus quadratus lumborum block on postoperative analgesia after pelvi-ureteric surgeries.

Detailed Description

Opioid-based analgesia plays a significant role in the control of postsurgical pain; however, use of opioid may lead to significant side effects (e.g., nausea and vomiting) and adverse events (e.g. respiratory depression), which may be associated with significantly longer hospital stays and higher hospital costs in the postsurgical setting .

Thoracic paravertebral block (TPVB) is a classic trunk block with definite analgesic effect for both somatic and visceral pain.

Quadratus Lumborum block (QLB) is a widely used regional anesthesia technique as well. It has been used for reducing postoperative pain after cesarean section, laparotomy or laparoscopic procedure and hip surgery.

Erector spinae plane block (ESPB) is a novel inter-fascial plane block first introduced by Forero et al. in 2016 , providing wide-ranging analgesia in lung surgery, laparoscopy, mastectomy, and pediatric surgery. The proposed mechanism of ESPB is that distribution of local anesthetic solution spreads into the para-vertebral space and epidural space, which then blocks the dorsal, ventral, and traffic branches of spinal nerve.

ESPB, TPVB and QLB III have been shown to improve analgesic outcome after urological surgeries.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
90
Inclusion Criteria
  • Age 18-65 years
  • Both genders
  • American Society of Anesthesiologists (ASA) physical status I-III
  • Undergoing elective pelvi-ureteric surgeries.
Exclusion Criteria
  • Body Mass Index > 30 kg/m2.
  • Contraindication of deep nerve block such as allergic to anesthetic drug, coagulation disorder, and infection at the injection site.
  • Chronic opioids dependence or chronic pain over 3 months.
  • Use of medication such as gabapentin-pregabalin could affect pain perception.
  • Unable to communicate preoperatively due to severe dementia, language barrier, or neuropsychiatric disorder.
  • Unable to perform nerve block procedure due to difficult anatomy through ultrasound scan.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
ESPB groupESPB Technique-
QLB groupQLB Technique-
TPVB groupTPVB Technique-
Primary Outcome Measures
NameTimeMethod
The total postoperative morphine consumption48 hours postoperatively

Total amount of rescue analgesic in the first 48 hours postoperative will be measured.

Secondary Outcome Measures
NameTimeMethod
Patients' satisfaction after surgery.48 hours Postoperatively

The degree of patient satisfaction will be assessed on a 5-point scale: (0= extremely dissatisfied, 1= unsatisfied, 2= neither satisfied nor unsatisfied, 3= satisfied), 4= extremely satisfied).

Access time of first analgesic48 hours Postoperatively

The time to first request of rescue analgesia will be recorded

Access post-operative pain scores48 hours Postoperatively

Postoperative pain will be accessed using Numeric Rating Scale which ranges from 0 to 10 points, with 0 indicating no pain, 1-3 indicating mild pain, 4-6 indicating moderate pain, and 7-10 indicating severe pain.

Trial Locations

Locations (1)

Mohammad Fouad Algyar

🇪🇬

Tanta, ElGharbiaa, Egypt

© Copyright 2025. All Rights Reserved by MedPath