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
NA
9 participants
INTERVENTIONAL
2004-09-30
2010-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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Ultrasound Pre-Arthrogram
Ultrasound of the joint(s) before the clinically scheduled arthrogram of the same joint(s)
Ultrasound
Ultrasound of the joint(s) before the clinically scheduled arthrogram of the same joint(s)
Ultrasound Post-Arthrogram
Ultrasound of the joint(s) after the clinically scheduled arthrogram of the same joint(s), performed while the body still has a contrast agent in it from the arthrogram. The contrast agent varies with different joint areas, but is usually iodine based (like Ultravist.)
Ultrasound
Ultrasound of the joint(s) after a clinically scheduled arthrogram is performed. Ultrasound images will then be compared to the arthrogram findings, other imaging findings such as MRI and surgical pathological findings such as arthroscopy (if any.)
Interventions
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Ultrasound
Ultrasound of the joint(s) before the clinically scheduled arthrogram of the same joint(s)
Ultrasound
Ultrasound of the joint(s) after a clinically scheduled arthrogram is performed. Ultrasound images will then be compared to the arthrogram findings, other imaging findings such as MRI and surgical pathological findings such as arthroscopy (if any.)
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* children under the age of 18
18 Years
ALL
No
Sponsors
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University of Michigan
OTHER
Responsible Party
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Jon Jacobson
Principal Investigator
Locations
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University of Michigan Hospital
Ann Arbor, Michigan, United States
Countries
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Other Identifiers
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2004-0761
Identifier Type: -
Identifier Source: org_study_id
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