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

Double Blinded Randomized Control Trial on the Effects of Ultrasound Probe Position on Ultrasound-guided Nerve Blocks

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01690156
Enrollment
62
Registered
2012-09-21
Start date
2012-08-31
Completion date
2013-02-28
Last updated
2024-01-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

In-plane Ultrasound-guided Regional Anesthesia Performance

Keywords

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

Brief 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.

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.

Interventions

None listed

Sponsors

University of New Mexico
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy volunteers * Right handed * Aged 18 to 55

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

Design outcomes

Primary

MeasureTime frameDescription
Time taken to perform a simulated interscalene block1 hourTime taken to perform a simulated interscalene block after watching an instructional video on ultrasound guided regional anesthesia on the simulated targets

Secondary

MeasureTime frameDescription
Duration where the entire needle is not visualized when performing the simulated interscalene block1 hourTime taken to perform a simulated interscalene block after watching an instructional video on ultrasound guided regional anesthesia on the simulated targets

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026