Musculoskeletal Ultrasound for Diagnosis of Shoulder Dislocation Reduction

NCT ID: NCT04703517

Last Updated: 2021-01-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-01-01

Study Completion Date

2021-12-30

Brief Summary

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This study will compare the current standard of care post reduction plain film x ray for confirmation of shoulder reduction to point of care ultrasound. Patients will receive both the current standard of care post reduction x ray and point of care ultrasound to act as their own comparators

Detailed Description

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Conditions

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Ultrasound Shoulder Dislocation Musculoskeletal Injury

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Self Controlled

Patients will active as their own comparator

Group Type OTHER

Point of care ultrasound

Intervention Type DIAGNOSTIC_TEST

Patients will receive a point of care ultrasound at the bedside in the Emergency Department and compare the impression to the x ray result

Interventions

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Point of care ultrasound

Patients will receive a point of care ultrasound at the bedside in the Emergency Department and compare the impression to the x ray result

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Adults greater than or equal to 18 years
* Acute shoulder dislocation

Exclusion Criteria

* Associated fracture
* Associated neurovascular injury
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Rutgers, The State University of New Jersey

OTHER

Sponsor Role lead

Responsible Party

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Jesper Aurup, MD

MD, Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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Jesper Aurup, MD

Role: CONTACT

732-258-9267

Other Identifiers

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Pro2020003069

Identifier Type: -

Identifier Source: org_study_id

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