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Trial registered on ANZCTR
Registration number
ACTRN12609000721202
Ethics application status
Approved
Date submitted
19/08/2009
Date registered
24/08/2009
Date last updated
9/07/2012
Type of registration
Retrospectively registered
Titles & IDs
Public title
Is bedside ultrasound a valuable tool for diagnosing common fractures in emergency department patients?
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Scientific title
Is bedside ultrasound a valuable tool for diagnosing common fractures in emergency department patients?
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Healthy patients with/without fractures.
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Condition category
Condition code
Musculoskeletal
239849
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0
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Other muscular and skeletal disorders
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Prospective convenience sampling of patients with suspected fracture of selected regions. Perform bedside ultrasonography using portable SONOSITE MicroMaxx ultrasound machine using a 12MHz transducer. Patients will be observed for 6 months.
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Intervention code [1]
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Diagnosis / Prognosis
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Comparator / control treatment
Comparing to diagnosis made from Xray/Computerised Tomography scan (CT)/Magnetic Resonance Imaging (MRI).
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Control group
Active
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Outcomes
Primary outcome [1]
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Sensitivity of using ultrasound to diagnose fractures.
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Assessment method [1]
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Timepoint [1]
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At completion of ultrasound scan and/or Xray/CT/MRI whichever is later.
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Primary outcome [2]
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Specificity of using ultrasound to diagnose fractures.
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Assessment method [2]
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Timepoint [2]
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At completion of ultrasound scan and/or Xray/CT/MRI whichever is later.
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Secondary outcome [1]
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To determine if time to correct diagnosis of the presence or absence of fracture can be reduced by the use of Ultrasound
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Assessment method [1]
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Timepoint [1]
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At completion of ultrasound scan and/or Xray/CT/MRI whichever is later.
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Eligibility
Key inclusion criteria
Patient with suspected fractures involving the metacarpal, distal radius/ulnar, olecranon, body of ulnar, clavicle, metatarsal, distal tibia/fibula, patella, proximal fibula, mandible or sternum.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Patient unable to give own consent
Patients with unstable, compound (open) or suspected open fractures
Haemodynamically unstable patients requiring urgent medical intervention
Patients with fracture dislocations requiring immediate relocation to avoid neurovascular compromisation
Enrolling clinician has already reviewed Xrays and made diagnosis prior performing ultrasound for the study
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Study design
Purpose
Natural history
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Duration
Cross-sectional
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Selection
Convenience sample
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
17/07/2009
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
500
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Self funded/Unfunded
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Name [1]
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Address [1]
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Country [1]
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Primary sponsor type
Individual
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Name
Ngee Wei Foo
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Address
Department of Emergency Medicine
Royal Adelaide Hospital
North Terrace
Adelaide
SA 5000
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Royal Adelaide Hospital Ethics Committee
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Ethics committee address [1]
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Royal Adelaide Hospital North Terrace Adelaide SA 5000
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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Approval date [1]
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02/07/2009
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Ethics approval number [1]
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RAH Protocol No 090702
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Summary
Brief summary
The primary purpose of this study is to determine if using a bedside ultrasound machine is as good as using an Xray to determine if a bone is fractured. A positive outcome from this study may speed up the treatment of patients with similar injuries and avoid unecessary exposure to radiation.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Dr. Ngee Wei Foo
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Address
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Department of Emergency Medicine
Royal Adelaide Hospital
North Terrace
Adelaide
SA 5000
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Country
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Australia
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Phone
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(+618) 82224000
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Dr. Ngee Wei Foo
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Address
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Department of Emergency Medicine
Royal Adelaide Hospital
North Terrace
Adelaide
SA 5000
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Country
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Australia
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Phone
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(+618) 82224000
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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