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TerminatedNCT01690156Updated Jan 10, 2024

Trial on the Effects of Ultrasound Probe Position on Ultrasound-guided Nerve Blocks

An observational study in In-plane Ultrasound-guided Regional Anesthesia Performance, sponsored by University of New Mexico. Terminated at 1 site in United States. Open to participants aged 18 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-01-10.

Sponsored by University of New Mexico · Observational

Why this study was terminated
This is not a clinical trial and was inadvertently entered in the system.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
62
Ages
18 Years to 55 Years
Sex
All
01

Study summary

Ultrasound has been used to guide a needle to inject local anesthetics around nerves. This is usually done in the same plane as the ultrasound beam in America and is known as an in-plane technique. When done correctly, the entire needle is visualized on the ultrasound screen as it approaches the nerves which are also seen on the same screen the entire time. The ultrasound probe can be held perpendicular or parallel to the shoulders of the person performing the in-plane technique. Our hypothesis is that holding the ultrasound probe perpendicular to the shoulder is superior to holding the probe parallel to the shoulder during an in-plane ultrasound guided regional anesthesia technique.

Read the detailed description

Right handed volunteers with no prior exposure to ultrasound techniques are used in this study. They will be randomly assigned to be shown an instructional video on how to perform an in-plane ultrasound guided needling technique on a realistic simulation target. The two videos are identical with the exception of the probe position. A blinded assessor will time the volunteers performance behind a screen and note the duration in which the needle is not visualized in the ultrasound screen.

02

Conditions studied

  • In-plane Ultrasound-guided Regional Anesthesia Performance

Keywords

  • In-plane
  • Ultrasound-guided regional anesthesia performance
  • Probe position
  • Needle visualization
03

In context

Lead sponsor

University of New Mexico is the lead sponsor of 306 studies on the registry; 28 are open to participants now.

Of its 25 completed or terminated interventional studies of FDA-regulated products, 23 (92%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Healthy volunteers naiive to ultrasound techniques

Inclusion criteria

  • Healthy volunteers
  • Right handed
  • Aged 18 to 55

Exclusion criteria

Exclusion Criteria:

  • Any person who has prior knowledge about ultrasound imaging or regional anesthesia
  • Any person who has prior experience with laparoscopy or biopsy
  • Any person who has problems with depth of field or simple hand eye co-ordination task
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
62 participants (actual)

Groups and cohorts

  • Parallel Probe Position

    Performing the simulated interscalene block with the ultrasound probe parallel to the shoulders of the person performing the block

  • Perpendicular Probe Position

    Performing the simulated interscalene block with the ultrasound probe perpendicular to the shoulders of the person performing the block

06

What researchers measure

Primary outcomes

  1. Time taken to perform a simulated interscalene block

    Time taken to perform a simulated interscalene block after watching an instructional video on ultrasound guided regional anesthesia on the simulated targets

    Time frame: 1 hour

Secondary outcomes

  1. Duration where the entire needle is not visualized when performing the simulated interscalene block

    Time taken to perform a simulated interscalene block after watching an instructional video on ultrasound guided regional anesthesia on the simulated targets

    Time frame: 1 hour

07

Study locations

1 site
  • University of New Mexico
    Albuquerque, New Mexico 87120, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 10, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01690156
Lead sponsor
University of New Mexico
Responsible party
Sponsor
First posted
Sep 21, 2012
Start date
Aug 2012
Primary completion
Feb 2013
Completion
Feb 2013
Last update
Jan 10, 2024

Study contacts

Nicholas C Lam, MD
principal investigator · University of New Mexico

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Jan 2024. You cannot join it, but the record below documents what was studied.

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