Operative Versus Nonoperative Treatment for Scapula Fractures
NCT ID: NCT00849771
Last Updated: 2015-11-13
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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WITHDRAWN
OBSERVATIONAL
2008-03-31
2009-01-31
Brief Summary
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The potential impact is a clearer set of choices in treatment options for this type of injury.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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1
Operative Treatment (Open Reduction Internal Fixation)
No interventions assigned to this group
2
Non-operative/Conservative Care
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Displacement of glenoid neck and scapula body of greater than 2 cm
* Angular deformity between the fracture fragments of greater than 45 degrees.
* A combination of displacement greater than 1.5 cm AND angulation greater than 30 degrees
* A glenopolar angle less than 22 degrees
* A Double Lesion of the Superior Shoulder Suspensory Complex (SSSC)
Exclusion Criteria
* Brachial Plexus Injury
* Traumatic Brain Injury or Cognitive Disability preventing participation in the consent or post injury rehabilitation
* Spinal cord injuries resulting in paraplegic, quadriplegic disabilities or permanent ipsilateral peripheral nerve damage
* Ipsilateral Upper Extremity Injury
* Previous Shoulder Surgery
* Insufficient English proficiency to complete the DASH Questionnaire
18 Years
ALL
No
Sponsors
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Vanderbilt University
OTHER
Responsible Party
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William Obremskey
Chief of Orthopedic Trauma
Principal Investigators
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William T. Obremskey, MD, MPH
Role: PRINCIPAL_INVESTIGATOR
Vanderbilt University Medical Center
Peter Cole, MD
Role: PRINCIPAL_INVESTIGATOR
University of Minnesota
Locations
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Vanderbilt Orthopaedic Institute, Vanderbilt University Medical Center
Nashville, Tennessee, United States
Countries
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Other Identifiers
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080160
Identifier Type: -
Identifier Source: org_study_id
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