Magnetic Resonance Imaging (MRI) Interpretations for Lumbar Spinal Stenosis (LSS)
NCT ID: NCT01017692
Last Updated: 2015-05-25
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
36 participants
OBSERVATIONAL
2009-06-30
2010-12-31
Brief Summary
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Detailed Description
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In this study 50-100 MRI studies of patients diagnosed with symptomatic lumbar spinal stenosis will be collected, de-identified, and assigned a study identification number for tracking purposes. Three "raters" from Upstate and three "rater" from outside the institution, that have experience reviewing MRI's will be asked to review the MRI's and classify the LSS at all lumbar levels as normal, mild, moderate or severe in the central canal, lateral recesses and the neuroforamen. The raters will not have any information about the patients. The MRI's will then be given a new identification number, and the patient's self-assessment questionnaires (which are also de-identified and given the study id number) will be given to the raters, for a second review. The raters will have the patients gender, age and outcomes scores from Short form 36, Visual Analog Scale, Oswestry Disability Index and Zurich Claudication Questionnaires. The raters will classify the MRI, as normal, mild, moderate or severe using the outcomes and information supplied.
The data from both ratings will be compiled and compared to assess the reliability of the radiologically established anatomical stenosis when compared with the subjects outcome scores.
This study is for current patients in Upstate Orthopedics office.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Lumbar Spinal Stenosis
Subjects who have undergone or will undergo an MRI, with symptoms of LSS
MRI
MRI of lumbar spine for subjects presenting with spinal stenosis symptoms
Interventions
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MRI
MRI of lumbar spine for subjects presenting with spinal stenosis symptoms
Eligibility Criteria
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Inclusion Criteria
* Must be able to undergo or have undergone an MRI of the Lumbar spine
* Must be able to read/understand English
* Must be a current patient in our practice
Exclusion Criteria
21 Years
ALL
No
Sponsors
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State University of New York - Upstate Medical University
OTHER
Responsible Party
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William Lavelle
Associate Professor
Principal Investigators
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William F Lavelle, MD
Role: PRINCIPAL_INVESTIGATOR
State University of New York - Upstate Medical University
Locations
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SUNY Upstate Medical University-Department of Orthopedics
Syracuse, New York, United States
Countries
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Other Identifiers
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5825-MRI Variability
Identifier Type: -
Identifier Source: org_study_id
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