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Clinical Trials/NCT04709211
NCT04709211
Completed
Not Applicable

A Comparative Study Between Postoperative Analgesia of Fascia Iliaca Compartment Block and Anterior Quadratus Lumborum Block in Proximal Femur Fracture

Ain Shams University1 site in 1 country128 target enrollmentJanuary 10, 2021

Overview

Phase
Not Applicable
Intervention
Facia Iliaca block
Conditions
Postoperative Pain
Sponsor
Ain Shams University
Enrollment
128
Locations
1
Primary Endpoint
first request of analgesia
Status
Completed
Last Updated
last year

Overview

Brief Summary

Fractures of the femur are common orthopaedic emergency especially in the geriatric population and central neuraxial blocks are the preferred technique for providing anaesthesia. However, limb immobility and extreme pain are the deterrents for ideal positioning for these procedures. postoperative pain is a nightmare so adequate analgesia has been advocated to reduce the pain. in this study, Facia Iliaca compartment block will be compared to anterior Quadratus lumborum block, both will be done Ultrasound-guided using Bupivacain0.25% for postoperative analgesia at the end of the surgery.

Detailed Description

In this prospective, randomized, comparative study patients will be equally divided into two equal groups; GroupI: patients will receive Ultrasound-guided Facia Iliaca compartment block with 50 ml 0.25%bupivacaine at the end of surgery Group Q: patients will receive Ultrasound-guided anterior Quadratus lumborum block with 50 ml 0.25%bupivacaine at the end of surgery

Registry
clinicaltrials.gov
Start Date
January 10, 2021
End Date
July 1, 2021
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Rania Maher Hussien, MD

Assistant professor of Anaesthesia

Ain Shams University

Eligibility Criteria

Inclusion Criteria

  • ASA II to IV
  • Both sexes
  • scheduled for fracture femur surgeries

Exclusion Criteria

  • patients with bleeding disorders and coagulopathy
  • infection at the injection site
  • known allergy to local anaesthetics
  • patients with multiple fractures
  • patients with pre-existing myopathy or neuropathy
  • patients with significant cognitive dysfunction
  • patients who receive long-acting opioids preoperatively

Arms & Interventions

Group I: Facia Iliaca block

patients will receive Ultrasound-guided Facia Iliaca Block using bupivacaine 0.25%

Intervention: Facia Iliaca block

Group Q: Anterior Quadratus lumbroum block

patients will receive Ultrasound-guided Anterior Quadratus Lumbroum block using bupivacaine 0.25%

Intervention: Anterior Quadratus Lumbroum block

Group Q: Anterior Quadratus lumbroum block

patients will receive Ultrasound-guided Anterior Quadratus Lumbroum block using bupivacaine 0.25%

Intervention: bupivacaine

Outcomes

Primary Outcomes

first request of analgesia

Time Frame: 48 hours postoperative

the time the patient felt pain and asked for analgesics

Secondary Outcomes

  • total opioid consumption(48 hours postoperative)

Study Sites (1)

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