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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00743600
Other study ID # HUM1500
Secondary ID
Status Completed
Phase N/A
First received August 27, 2008
Last updated November 8, 2016
Start date September 2005
Est. completion date December 2013

Study information

Verified date November 2016
Source University of Michigan
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study will use healthy volunteers and patients with shoulder problems (pain or impaired movement). Ultrasound will be used to image and document the appearance of both normal and abnormal shoulder structures.


Description:

The purpose of this study is to document normal and abnormal appearances of various shoulder structures (rotator cable and rotator cuff).

This study will recruit healthy volunteers and patients who have been referred to Radiology for a symptomatic shoulder (a shoulder that is causing the patient pain, or is limited in its ability to move.) Both groups will undergo ultrasound imaging of the shoulder.


Recruitment information / eligibility

Status Completed
Enrollment 123
Est. completion date December 2013
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with shoulder pain referred to radiology for ultrasound of shoulder

Exclusion Criteria:

- Patients less than 18 years of age

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Other:
ultrasound of painful shoulder
Patients who have a shoulder that is painful or has limited movement who were referred to Radiology will have an ultrasound exam of their shoulder.
ultrasound
Healthy volunteers who do not have pain or limited movement will have an ultrasound exam of their shoulder.

Locations

Country Name City State
United States University of Michigan Health System Ann Arbor Michigan

Sponsors (1)

Lead Sponsor Collaborator
University of Michigan

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To determine if Ultrasound can identify the rotator cable and the associated structures. 1 year No
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