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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02688205
Other study ID # 20140107R
Secondary ID SKH-8302-103-DR-
Status Completed
Phase
First received
Last updated
Start date March 2014
Est. completion date December 2015

Study information

Verified date February 2016
Source Shin Kong Wu Ho-Su Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Shoulder problems cause substantial disability in daily living, work, leisure activity, and exercise. The presence of shoulder problem such as rotator cuff pathology reported was highly predictive of impaired health-related quality of life. Many tests were used for physical examination of the shoulder. The reliability and validity of the tests have been studied before. However, a systemic review concluded that there was conflicting evidence in reliability of each or combined tests. Functional examination of the shoulder by Cyriax is composed of a series of tests to evaluate a shoulder problem. It includes three arm elevation, three tests for glenohumeral joints, and six resisted tests. As far as the investigators know, correlation of Cyriax functional examination with the ultrasonographic findings has never been reported before. Therefore, the aim of this study is to compare the clinical diagnosis by Cyriax's functional examination with ultrasound findings in patients with shoulder pain.


Description:

There are two groups with fifty patients in each group. First group is patients who have unilateral or bilateral shoulder pain from the outpatient clinic of Department of Physical Medicine and Rehabilitation in Shin Kong Wu Ho-Su Memorial Hospital. The other group is control group who has no shoulder problems. Both groups will receive Cyriax's functional examination of the shoulder after history taking, and will be examined by shoulder ultrasound in one week.


Recruitment information / eligibility

Status Completed
Enrollment 206
Est. completion date December 2015
Est. primary completion date June 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: Study group: 1. patients with unilateral or bilateral shoulder pain with unknown causes; 2. age= 20 years old. Control group: 1. patients without unilateral or bilateral shoulder pain; 2. age= 20 years old. Exclusion Criteria: 1) chronic inflammatory joint disease, infections or tumors of the shoulder, previous fracture or surgery of shoulder, and referred pain from cervical origin or visceral organs.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Cyriax's functional examination
included active range of motion, passive range of motion, resisted test and accessory test for shoulder pain evaluation
Device:
Ultrasound examination
to evaluate rotator cuff, acromio-clavicular joint, and subdeltoid-subacromial bursa

Locations

Country Name City State
Taiwan Shin Kong Wu Ho-Su Memorial Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
Shin Kong Wu Ho-Su Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cyriax's functional examination for diagnosis After Cyriax's functional examination for evaluating shoulder pain, a clinical diagnosis is made by the physician 1 week
Primary Ultrasound examination for diagnosis Ultrasound examination is done in one week after Cyriax's functional examination for detailed shoulder pathology evaluation. 1 week
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