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Pocket Sized Ultrasound (PsUS) and Pediatric Elbow Fractures

Primary Purpose

Elbow Injury, Elbow Fracture

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Butterfly IQ
Sponsored by
University of Chicago
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Elbow Injury focused on measuring Pocket sized ultrasound, Pediatric elbow injury, Pediatric elbow fracture

Eligibility Criteria

1 Year - 16 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria: For Feasibility phase: children between the ages of 1-16 years olds For Active phase: children between the ages of 1-16 years olds with isolated, acute (less than 48 hrs) elbow pain in the setting of adequate history of trauma Exclusion Criteria: Both phases: Children <1 or >16 years old Those with open fractures, gross deformities, multiple traumatic injuries, distal neurovascular compromise, unstable vital signs or hemodynamic instability, altered mental status, history of skeletal abnormalities, or past elbow fracture as well as wards of the state or those unable to provide consent Patients who have a confirmed diagnosis of fracture at an outside institutions prior to arrival to the ED will also be excluded

Sites / Locations

  • University of Chicago/Comer Children's Hospital

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Ultrasound Exam

Arm Description

Every participant will undergo a pocket-sized ultrasound exam. The comparison to these images will either be a X-ray if fracture is suspected or bedside nursemaid reduction if subluxation is suspected (participants will act as their own comparison based not their routine ED clinical management)

Outcomes

Primary Outcome Measures

Accuracy of pocket sized ultrasound elbow exams compared to Xray in suspected fracture or bedside nursemaid reduction in suspected subluxations.
Images will be categorized as positive, negative or equivocal for signs of fracture. Accuracy will be determined be determined will be sensitivity and specificity, negative and positive predictive value, using Xray or performance of bedside nursemaid reduction as gold standard comparison.

Secondary Outcome Measures

Feasibility of the study training and protocol for adequate image capture
Feasibility outcome and acceptability of study training will be determined by successful completion of adequate images obtain during ultrasound elbow exam which will be determine during internal review of images. Images will deemed adequate or inadequate for interpretation

Full Information

First Posted
April 4, 2023
Last Updated
May 17, 2023
Sponsor
University of Chicago
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1. Study Identification

Unique Protocol Identification Number
NCT05870345
Brief Title
Pocket Sized Ultrasound (PsUS) and Pediatric Elbow Fractures
Official Title
The Diagnostic Accuracy of Pocket Size Ultrasound (PsUS) in the Detection of Pediatric Elbow Fractures
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 18, 2022 (Actual)
Primary Completion Date
May 5, 2023 (Actual)
Study Completion Date
June 7, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Chicago

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes

5. Study Description

Brief Summary
The main purpose of this project is to investigate the accuracy of pocket-sized ultrasound (PsUS) in the diagnosis of pediatric elbow fractures. The primary research objective is to determine the test performance characteristics of PSUS performed by pediatric emergency medicine physicians compared to radiography for the detection of pediatric elbow fractures. The project will consist of two parts, first involving a feasibility study and followed by an active study. The feasibility study will aim to answer if providers can perform an adequate elbow ultrasound exam after a brief study training. The active study will investigate the initial accuracy of the PsUS. Participants will be asked in either the feasibility or the active phases of the study to undergo a brief pocket-sized ultrasound elbow exam of both elbows. Patient will continue to receive their previously determined clinical ED management. In the active phase of the study, participant's elbow X-rays or if patient underwent bedside nursemaid reduction will be the comparison to pocket-sized ultrasound images.
Detailed Description
The main purpose of this project is to investigate the accuracy of pocket-sized ultrasound (PsUS) in the diagnosis of pediatric elbow fractures. The primary research objective is to determine the test performance characteristics of PSUS performed by pediatric emergency medicine physicians compared to radiography for the detection of pediatric elbow fractures. The project will consist of two parts, first involving a feasibility study and followed by an active study. This project will consist of two parts, involving first a brief feasibility phase followed by a pilot study conducted in an urban pediatric emergency department (Comer Children's Hospital in Chicago, IL). For the feasibility phase, the purpose is to demonstrate that novice PsUS users are able to obtain accurate and adequate imaging for interpretation. This phase will initially involve the study providers receiving the elbow PsUS exam training. Once trained, each study provider will obtain 3 elbow exams of participants between the ages of 1-16 years old. Providers will use the standardized views reviewed in the ultrasound training to perform the exam, with verbal consent obtained from each participant's parent for inclusion in the feasibility study. These images will be reviewed by study staff to ensure US examiners are obtaining the correct standardized views. Once the feasibility exams are completed, the study providers are able to begin active study recruitment which will involve recruiting children between the ages of 1-16 years old with isolated acute elbow pain. Parents will initially be approached in the emergency department (ED), with written consent obtained if interested and eligible. Once consented, patients will undergo bilaterally standardized elbow exams using the pocket-sized ultrasound. All images will be stored on a password protected, cloud-based imaging database with all identifying information removed. After the exam, a basic assessment of the images will be made by the bedside ultrasound provider, as positive, negative or equivocal for signs of elbow fracture, but before reviewing any radiographic imaging. A positive PsUS will be defined as the presence of signs of elbow fracture, either as direct signs including cortical discontinuities or indirect signs including posterior fat pad with or without lipohemarthrosis on ultrasound exam. Following the ultrasound exam, patients will undergo standard clinical care for acute elbow injury per primary ED team which may consist of Xray or possible bedside nursemaid reduction. When applicable, study investigators will review the final blinded radiology readings of the initial or subsequent x-ray images after the patient encounter. Additionally, research staff will also attempt to follow up with participants after their ED visit for their elbow injury to determine if any additional radiographic imaging or care was obtained and if subsequent occult fractures were discovered on later imaging that may have been missed on the initial evaluation. The primary aim of the feasibility portion of the study is to determine acceptability of the PsUS study training to obtain adequate elbow images. The primary aim of the active study is to compare the initial test performance characteristics of PSUS performed by bedside physicians compared to standard radiography in the diagnosis of pediatric elbow fractures.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Elbow Injury, Elbow Fracture
Keywords
Pocket sized ultrasound, Pediatric elbow injury, Pediatric elbow fracture

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Each participant receives the study intervention which is a pocket-sized ultrasound exam.
Masking
None (Open Label)
Allocation
N/A
Enrollment
13 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ultrasound Exam
Arm Type
Other
Arm Description
Every participant will undergo a pocket-sized ultrasound exam. The comparison to these images will either be a X-ray if fracture is suspected or bedside nursemaid reduction if subluxation is suspected (participants will act as their own comparison based not their routine ED clinical management)
Intervention Type
Device
Intervention Name(s)
Butterfly IQ
Intervention Description
Butterfly IQ is a pocket sized ultrasound device. Each participant will undergo a ultrasound exam of both elbows using a pocket sized ultrasound device.
Primary Outcome Measure Information:
Title
Accuracy of pocket sized ultrasound elbow exams compared to Xray in suspected fracture or bedside nursemaid reduction in suspected subluxations.
Description
Images will be categorized as positive, negative or equivocal for signs of fracture. Accuracy will be determined be determined will be sensitivity and specificity, negative and positive predictive value, using Xray or performance of bedside nursemaid reduction as gold standard comparison.
Time Frame
1ED visit (1 day)
Secondary Outcome Measure Information:
Title
Feasibility of the study training and protocol for adequate image capture
Description
Feasibility outcome and acceptability of study training will be determined by successful completion of adequate images obtain during ultrasound elbow exam which will be determine during internal review of images. Images will deemed adequate or inadequate for interpretation
Time Frame
Over brief time period for 3 completed ultrasound exams, approximately < 3 hrs

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: For Feasibility phase: children between the ages of 1-16 years olds For Active phase: children between the ages of 1-16 years olds with isolated, acute (less than 48 hrs) elbow pain in the setting of adequate history of trauma Exclusion Criteria: Both phases: Children <1 or >16 years old Those with open fractures, gross deformities, multiple traumatic injuries, distal neurovascular compromise, unstable vital signs or hemodynamic instability, altered mental status, history of skeletal abnormalities, or past elbow fracture as well as wards of the state or those unable to provide consent Patients who have a confirmed diagnosis of fracture at an outside institutions prior to arrival to the ED will also be excluded
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Holly Benjamin, MD
Organizational Affiliation
University of Chicago/Comer Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Chicago/Comer Children's Hospital
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60637
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
This study does not plan to share information with other researchers
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Pocket Sized Ultrasound (PsUS) and Pediatric Elbow Fractures

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