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Completed

NCT Number: NCT03805906

Ultrasound-guided L5 Dorsal Ramus Block

This study will examine the accuracy of an ultrasound-guided L5 dorsal ramus block technique.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Kelowna General Hospital

Kelowna, British Columbia, V1Y 1T2, Canada

About this study

The lumbar facet joints have been implicated as a causal factor in 15 to 40% of patients suffering from chronic low back pain. Because physical examination and medical imaging have limited value in determining the source of pain, diagnostic blocks play an important role in the management of this common condition. Blocks of the L5 dorsal ramus (DR) are used to diagnosed pain originating from the L5-S1 facet joint, which is one of the most commonly implicated levels in patients with low back pain. Fluoroscopic guidance, which uses x-rays, is currently the standard imaging modality used to perform this block. Recently, ultrasound guidance has seen increasing use because of its greater accessibility and lack of ionizing radiation. Although USG has been shown to provide a high level of accuracy at other levels, the greater anatomical complexity found at the L5-S1 has hindered the development of a satisfactory L5 DR block technique. In this study the investigators will use fluoroscopic control to examine the accuracy of a novel ultrasound-guided approach to this block.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

-Any consenting patient over 18 years of age with axial low back pain who requires a diagnostic L5 dorsal ramus block.

Exclusion criteria

  • Inability to consent
  • Iodine or lidocaine allergy,
  • Pregnancy,
  • Coagulopathy (as defined by an INR over 1.4, platelets under 100,000, or a documented bleeding disorder)
  • Inability to visualize lumbosacral anatomy during an ultrasound pre- scan

Treatment and study plan

L5 Dorsal ramus block

Procedure

Ultrasound-guided L5 dorsal ramus block

Primary outcomes

  1. Block accuracy

    Time frame: Immediately post-injection

    contrast distribution

Secondary outcomes

  1. Performance time

    Time frame: Perioperative

    Performance time as defined by the time the first image is acquired until the time the contrast injection is completed.

  2. Number of needle passes

    Time frame: Procedure

    Number of needle passes required to perform block

Sponsors and collaborators

Lead sponsor

Montreal General Hospital

Other

Collaborators

  • Kelowna General Hospital
  • University of British Columbia

Registry information

Official study title

Ultrasound-guided L5 Dorsal Ramus Block: Description and Validation of a Novel Technique

Acronym: USGL5DR

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Jan 16, 2019
Registry last updated
Sep 16, 2020

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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