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Efficient Anterior Shoulder Ultrasound Reduction Multicenter Prospective Randomized Trial (EASiUR)

Virginia Commonwealth University (VCU) logo

Virginia Commonwealth University (VCU)

Status

Terminated

Conditions

Shoulder Dislocation

Treatments

Diagnostic Test: Ultrasound
Diagnostic Test: X-Ray

Study type

Interventional

Funder types

Other

Identifiers

NCT04820491
HM20019991

Details and patient eligibility

About

The purpose of the study is to determine if using ultrasound to diagnosis and confirm reductions of shoulder dislocations impacts the length of an emergency department visit for this condition.

Full description

The purpose of the study is to determine if the length of the emergency department visit can be decreased and if patient exposure to x-rays can be reduced by utilizing an ultrasound to diagnose and confirm reduction in shoulder dislocations.

This study also seeks to determine if patients prefer ultrasound to x-ray when used to treat their shoulder dislocation.

Participants will be randomly assigned to one of two groups: either x-rays or ultrasound for the diagnosis and reduction confirmation of your shoulder dislocation.

Participant's shoulder dislocation will be treated per standard of care.

Participants will be asked to complete a short survey at the end of their visit.

Enrollment

9 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients who are 18 years of age or older; and
  2. Present to the VCU Emergency Department; and
  3. Have clinical signs of uncomplicated shoulder dislocation; and
  4. Agree to participation in the study; and
  5. Provides a written consent to be included in the study.

Exclusion criteria

  1. Patients who have a level 1 or 2 trauma activation, and/or;
  2. Patients who are pregnant, incarcerated, or unable to consent, and/or;
  3. Patients who have a past medical history of shoulder replacement in dislocated shoulder; and/or
  4. Provider Discretion

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

9 participants in 2 patient groups

X-Ray
Active Comparator group
Treatment:
Diagnostic Test: X-Ray
Ultrasound
Active Comparator group
Treatment:
Diagnostic Test: Ultrasound

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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