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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04820491
Other study ID # HM20019991
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date March 26, 2021
Est. completion date October 21, 2021

Study information

Verified date October 2022
Source Virginia Commonwealth University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Terminated
Enrollment 9
Est. completion date October 21, 2021
Est. primary completion date October 21, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
X-Ray
Shoulder x-rays as felt necessary for standard of care of diagnosis of shoulder dislocation and reduction
Ultrasound
Initial evaluation with ultrasound; may also evaluate nearby areas for concern of fracture. Order x- rays after ultrasound as seen fit for other injuries of diagnostic uncertainty.

Locations

Country Name City State
United States Virginia Commonwealth University Richmond Virginia

Sponsors (1)

Lead Sponsor Collaborator
Virginia Commonwealth University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Length of Stay in the Emergency Department (ED) Length of stay in the ED will be calculated from time of first provider contact to time of discharge from the ED. up to 8 hours or time to admission
Secondary Patient Satisfaction Patient satisfaction will be assessed using a 6 item scale. Each item is rated from 1 (extremely dissatisfied) to 5 (extremely satisfied). Scores are summed yielding scores ranging from 6 (most dissatisfied) to 30 (most satisfied). at discharge or admission - up to 8 hours
Secondary Time to Diagnosis Time to diagnosis will be calculated from time of first provider contact to time of x-ray or time of ultrasound per treatment condition up to 8 hours or time to admission
Secondary Confirmation of Reduction As documented by x-ray or ultrasound per treatment condition up to 8 hours or time to admission
Secondary Cost of Treatment Calculated as total billing cost of procedures related to shoulder dislocation ED visit up to 8 hours or time to admission
Secondary Total Number of Xrays Total number of xrays ordered during time in ED up to 8 hours or time to admission
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