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OpenTrials
Completed

NCT Number: NCT04709211

Fascia Iliaca Compartment Block Versus Anterior Quadratus Lumborum Block

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.

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Key information

Age range

50 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ain Shams University

Cairo, Abassia, Egypt

About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Facia Iliaca block

Procedure

patients will receive Ultrasound-guided Facia Iliaca block using 50 ml 0f Bupivacaine 0.25%

Anterior Quadratus Lumbroum block

Procedure

patients will receive Ultrasound-guided Anterior Quadratus Lumbroum block using 50 ml 0f Bupivacaine 0.25%

Bupivacaine

Drug

bupivacaine

Primary outcomes

  1. first request of analgesia

    Time frame: 48 hours postoperative

    the time the patient felt pain and asked for analgesics

Secondary outcomes

  1. total opioid consumption

    Time frame: 48 hours postoperative

    total dose of fentanyl used

Sponsors and collaborators

Lead sponsor

Ain Shams University

Other

Registry information

Official study title

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

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Jan 14, 2021
Registry last updated
Oct 9, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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