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Time to Diagnosis of Glenohumeral Joint Dislocations in the ED- Traditional Radiography vs. POC Ultrasound

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University of Nebraska

Status

Withdrawn

Conditions

Glenohumeral Dislocation

Treatments

Procedure: Shoulder reduction

Study type

Interventional

Funder types

Other

Identifiers

NCT05237167
0790-21-FB

Details and patient eligibility

About

This is study to compare the time to diagnosis of glenohumeral joint dislocation using two imaging methods, traditional x-ray and point-of-care ultrasound. Participants who present at the emergency department complaining of shoulder injury and who are suspected of having a possible glenohumeral shoulder dislocation will be eligible for the study. A reduction of the joint will be performed if imaging findings so indicate. All participants will receive a post-reduction x-ray and be referred to appropriate follow-up care.

Full description

This is a prospective comparison study evaluating the time to diagnosis of glenohumeral joint dislocation using two imaging modalities, traditional x-ray and point-of-care ultrasound. Eligible participants will include those who present to the emergency department with complaints of shoulder injury who are suspected by triage nursing of having a possible glenohumeral shoulder dislocation. Eligible participants will be consented by participating physicians and randomized into ultrasound or x-ray groups. If indicated based on the imaging findings, a reduction of the joint will be performed. All patients will receive a post-reduction x-ray and be referred to appropriate follow-up care based on the findings of their evaluation.

Sex

All

Ages

19+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adult patients (19 and older in state of Nebraska) who present to the emergency department with shoulder pain/injury and potential shoulder dislocation

Exclusion criteria

  • Injury sustained in major traumatic event (trauma activation), unable to consent, in extremis, less then 19 years of age

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

Ultrasound
Experimental group
Description:
After randomization, these subjects will undergo diagnostic point-of-care ultrasound
Treatment:
Procedure: Shoulder reduction
Radiograph
Active Comparator group
Description:
After randomization, these subjects will undergo diagnostic plain radiograph
Treatment:
Procedure: Shoulder reduction

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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