Ultrasound Examination and Guided Injection Into the Acromio-clavicular Joint
Primary Purpose
Osteoarthritis of Acromioclavicular Joint
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
contrast material injection
Sponsored by
About this trial
This is an interventional diagnostic trial for Osteoarthritis of Acromioclavicular Joint
Eligibility Criteria
Inclusion Criteria:
- adults over 18 years with AC joint degenerative changes
Sites / Locations
Outcomes
Primary Outcome Measures
ultrasound controlled injection of contrast material into the AC joint followed by standard x-ray
standard x-ray will be taken after the contrast dye has been injected into the joint to see whether it has successfully been placed into the joint.
Secondary Outcome Measures
Full Information
NCT ID
NCT01628796
First Posted
June 19, 2012
Last Updated
June 26, 2012
Sponsor
The Baruch Padeh Medical Center, Poriya
1. Study Identification
Unique Protocol Identification Number
NCT01628796
Brief Title
Ultrasound Examination and Guided Injection Into the Acromio-clavicular Joint
Official Title
Ultrasound Measurement of the Acromio-clavicular Joint and Injection of Standard Contrast Material Into the Joint Under Ultrasonic Control
Study Type
Interventional
2. Study Status
Record Verification Date
June 2012
Overall Recruitment Status
Unknown status
Study Start Date
July 2012 (undefined)
Primary Completion Date
January 2013 (Anticipated)
Study Completion Date
January 2013 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Baruch Padeh Medical Center, Poriya
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Is it possible to improve the accuracy of injection into the acromio-clavicular joint with the use of ultrasound?
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis of Acromioclavicular Joint
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Other
Intervention Name(s)
contrast material injection
Other Intervention Name(s)
iomeron 350
Intervention Description
using ultrasound to locate ac joint and injecting contrast material to ensure that the dye is actually in the joint
Primary Outcome Measure Information:
Title
ultrasound controlled injection of contrast material into the AC joint followed by standard x-ray
Description
standard x-ray will be taken after the contrast dye has been injected into the joint to see whether it has successfully been placed into the joint.
Time Frame
outcome assessed at the time of the injection (1 day)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
adults over 18 years with AC joint degenerative changes
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gordon Edelson, MD
Phone
97246652670
Email
edelson@bezeqint.net
12. IPD Sharing Statement
Learn more about this trial
Ultrasound Examination and Guided Injection Into the Acromio-clavicular Joint
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