Musculoskeletal Pain Clinical Trial
Official title:
Comparison of Clinical and Ultrasonographic Parameters of Rotator Cuff Tendinopathy Patients With and Without Nocturnal Pain
Verified date | March 2018 |
Source | Suleyman Demirel University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This study aimed to investigate the effects of nocturnal pain on clinical and ultrasonographic parameters in patients with rotator cuff tendinopathy.
Status | Completed |
Enrollment | 90 |
Est. completion date | October 15, 2017 |
Est. primary completion date | July 1, 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients aged over 18 years diagnosed with rotator cuff tendinopathy Exclusion Criteria: - Severe limitation and pain in head and neck movements - Loss of strength - Sensation and reflexes loss in the upper extremity - Limitation in passive shoulder movements on physical examination - Systemic rheumatic disease - Diabetes mellitus - Malignant disease - Active infection - Intraarticular injection - Trauma - Dementia - History of surgery - Bilateral should pain - Psychiatric discomfort - Smoking history - Antiinflammatory drugs or received physical therapy within the last 3 months - Beck depression score of higher than 13. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Suleyman Demirel University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Anterior circumflex humeral artery peak systolic velocity | Ultrasonographic examination | 1 week | |
Primary | Anterior circumflex humeral artery resistive index | Ultrasonographic examination | 1 week |
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