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Clinical Trials/NCT04541732
NCT04541732
Completed
Not Applicable

Ultra-sound Guided Bilateral Quadratus Lumborum Block Versus Epidural Block for Postoperative Analgesia After Major Abdominal Surgeries.

Mansoura University1 site in 1 country80 target enrollmentJanuary 1, 2019

Overview

Phase
Not Applicable
Intervention
Thoracic epidural block
Conditions
Elective Major Abdominal Surgery
Sponsor
Mansoura University
Enrollment
80
Locations
1
Primary Endpoint
Postoperative 24 hours cumulative rescue morphine consumption
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Acute postoperative pain is an important issue after major abdominal surgeries for which different analgesic modalities have been tried.

Epidural analgesia is the recommended technique to relieve pain after major abdominal surgeries owing to the proved superior analgesia, reduction of opioid-related side effects as nausea, vomiting, pruritis and sedation, earlier recovery of bowel function and earlier ability for postoperative mobility. However, it is not without complications.

Quadratus lumborum block is an ultrasound-guided block that provides patients with both visceral and somatic blockade. It lessens the potential risks associated with neuraxial techniques, so it may represent a novel alternative approach for analgesia after major abdominal surgeries.

Detailed Description

The aim of this study is to detect the feasibility of ultra-sound guided bilateral quadratus lumborum block as a postoperative analgesic modality after major abdominal surgery in comparison to epidural block and its effects on total rescue analgesic requirements in the 1st postoperative 24hours, time to first analgesic request, pain VAS scores, intraoperative and postoperative hemodynamics and postoperative opioid-related side effects. Under complete aseptic conditions, the patients will receive either thoracic epidural block or bilateral ultrasound-guided quadratus lumborum block after induction of general anaesthesia

Registry
clinicaltrials.gov
Start Date
January 1, 2019
End Date
May 6, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • American Society of Anesthesiologists (ASA) physical status I-III

Exclusion Criteria

  • Patient's refusal
  • Significant cardiac, disease.
  • Significant hepatic disease.
  • Significant renal disease (serum creatinine ˃ 1.5 mg/dl).
  • Patients with drug abuse
  • Allergy to study medications
  • Mental disease
  • Communication barrier.
  • Coagulopathy.
  • Local skin infection

Arms & Interventions

Thoracic epidural block

Patients will receive thoracic epidural block following induction of general anaesthesia

Intervention: Thoracic epidural block

Thoracic epidural block

Patients will receive thoracic epidural block following induction of general anaesthesia

Intervention: Induction of general anaesthesia with propofol

Thoracic epidural block

Patients will receive thoracic epidural block following induction of general anaesthesia

Intervention: Muscle Relaxant

Thoracic epidural block

Patients will receive thoracic epidural block following induction of general anaesthesia

Intervention: Maintenance of general anaesthesia

Bilateral quadratus lumborum block

Patients will receive Ultrasound-guided bilateral quadratus lumborum block following induction of general anaesthesia

Intervention: Ultrasound-guided bilateral quadratus lumborum block

Bilateral quadratus lumborum block

Patients will receive Ultrasound-guided bilateral quadratus lumborum block following induction of general anaesthesia

Intervention: Induction of general anaesthesia with propofol

Bilateral quadratus lumborum block

Patients will receive Ultrasound-guided bilateral quadratus lumborum block following induction of general anaesthesia

Intervention: Muscle Relaxant

Bilateral quadratus lumborum block

Patients will receive Ultrasound-guided bilateral quadratus lumborum block following induction of general anaesthesia

Intervention: Maintenance of general anaesthesia

Outcomes

Primary Outcomes

Postoperative 24 hours cumulative rescue morphine consumption

Time Frame: For 24 hours after surgery

Secondary Outcomes

  • The duration of postoperative analgesia(For 24 hours after surgery)
  • Postoperative pain score at rest(For 24 hours after surgery)
  • Systolic blood pressure(For 28 hours after induction of anesthesia)
  • Postoperative pain score on movement(For 24 hours after surgery)
  • Heart rate(For 28 hours after induction of anesthesia)
  • Degree of postoperative nausea and vomiting(For 24 hours after surgery)
  • Pruritis(For 24 hours after surgery)
  • Postoperative pain score on cough(For 24 hours after surgery)
  • Diastolic blood pressure(For 28 hours after induction of anesthesia)
  • Mean blood pressure(For 28 hours after induction of anesthesia)

Study Sites (1)

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