The Effect of Point-of-care Ultrasound Guidance for Distal Radius Fracture Reduction

NCT ID: NCT02962206

Last Updated: 2024-07-29

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

COMPLETED

Clinical Phase

NA

Total Enrollment

22 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-01-10

Study Completion Date

2018-06-30

Brief Summary

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Distal radius (Colle's) fractures in adult patients are commonly reduced in the emergency department before casting. Standard of care currently requires that x-rays be performed before and after fracture reduction, and inadequate reductions may be subject to repeat attempts and are at a higher risk to require surgery. This study will assess the use of point-of-care ultrasound (POCUS) in addition to standard care as a tool to decrease the angulation at the fracture site after a reduction is performed. If this angulation is decreased, it would suggest that POCUS for distal radius fracture reduction could decrease the number of failed reduction attempts and therefore the number of repeated reduction attempts.

Detailed Description

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Conditions

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Point-of-care Ultrasound, Distal Radius Fracture

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Standard of care

Patients will undergo standard closed fracture reduction. The sedation type, reduction method, and immobilization method will be at the discretion of the treating physician. Point-of-care ultrasound will not be used.

Group Type ACTIVE_COMPARATOR

Closed fracture reduction

Intervention Type PROCEDURE

The distal radius fracture will be reduced with using a combination of local anesthetic, sedation, reduction maneouvers and immobiliazation at the discretion of the treating physician

Experimental Group

Patients will undergo standard closed fracture reduction with the addition of point-of-care ultrasound use to assess post-reduction dorsal angulation. The sedation type, reduction method, and immobilization method will be at the discretion of the treating physician.

Group Type EXPERIMENTAL

Point-of-care ultrasound

Intervention Type DEVICE

After the fracture reduction maneouver, the physician will assess residual dorsal angulation using point-of-care ultrasound. If deemed adequate, the physician will progress to immobilization. If the reduction is not adequate, the physician will attempt further reduction at their discretion.

Closed fracture reduction

Intervention Type PROCEDURE

The distal radius fracture will be reduced with using a combination of local anesthetic, sedation, reduction maneouvers and immobiliazation at the discretion of the treating physician

Interventions

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Point-of-care ultrasound

After the fracture reduction maneouver, the physician will assess residual dorsal angulation using point-of-care ultrasound. If deemed adequate, the physician will progress to immobilization. If the reduction is not adequate, the physician will attempt further reduction at their discretion.

Intervention Type DEVICE

Closed fracture reduction

The distal radius fracture will be reduced with using a combination of local anesthetic, sedation, reduction maneouvers and immobiliazation at the discretion of the treating physician

Intervention Type PROCEDURE

Other Intervention Names

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POCUS

Eligibility Criteria

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Inclusion Criteria

* radiographically confirmed distal radius fracture

Exclusion Criteria

* patients who do not consent
* patients with multiple acute injuries, open fractures, or other local fractures evident (a simple ulnar styloid fracture will not be considered an exclusion criterion)
* patients with neurovascular compromise
* patients with bilateral distal radius fractures
* patients with minimally displaced distal radius fractures that do not require closed reduction before casting
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

OTHER

Sponsor Role collaborator

Marcus Van Aarsen

OTHER

Sponsor Role lead

Responsible Party

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Marcus Van Aarsen

Resident Physician

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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St. Joseph's Health Care London

London, Ontario, Canada

Site Status

London Health Sciences Centre

London, Ontario, Canada

Site Status

Countries

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Canada

Other Identifiers

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107331

Identifier Type: -

Identifier Source: org_study_id

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