Evaluating Validity of Ultrasonography in Determining Distal Radius Fracture Reduction
NCT ID: NCT01823692
Last Updated: 2013-04-04
Study Results
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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COMPLETED
PHASE2
184 participants
INTERVENTIONAL
2011-09-30
2011-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
SINGLE
Study Groups
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Distal Radius Fracture
after manipulation and reduction were performed by single emergency medicine specialist under Bier block regional anesthesia or procedural sedation-analgesia, The ultrasonography was performed by the single emergency department physician in a long axis both in a anterioposterior and lateral views in determining whether the distal and proximal distal to a fracture was in a straight line (less than 3 mm difference) or not?
ultrasonography
after manipulation and reduction were performed by single emergency medicine specialist under Bier block regional anesthesia or procedural sedation-analgesia, The ultrasonography was performed by the single emergency department physician in a long axis both in a anterioposterior and lateral views in determining whether the distal and proximal distal to a fracture was in a straight line (less than 3 mm difference) or not?
Interventions
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ultrasonography
after manipulation and reduction were performed by single emergency medicine specialist under Bier block regional anesthesia or procedural sedation-analgesia, The ultrasonography was performed by the single emergency department physician in a long axis both in a anterioposterior and lateral views in determining whether the distal and proximal distal to a fracture was in a straight line (less than 3 mm difference) or not?
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* more than 20 degree angulation
* joint internal involvement, communicated and along with Neurovascular compromised fractures
* patient's surgery due to other causes
* need to stay in the ICU and not being able to be treated at the same time for distal radius fracture
* patient's refusal to participate in the study
21 Years
ALL
Yes
Sponsors
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Isfahan University of Medical Sciences
OTHER
Responsible Party
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Hamidreza Shemshaki
MD, Research Assistant
Principal Investigators
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Hamidreza Shemshaki, MD
Role: PRINCIPAL_INVESTIGATOR
Isfahan University of Medical Sciences
Locations
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Al-Zahra University Hospital
Isfahan, Isfahan, Iran
Countries
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Other Identifiers
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ASD-1213-75
Identifier Type: -
Identifier Source: org_study_id
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