Clinical Trial

Subacromial Impingement Syndrome Functional Tests Correlation With Ultrasound Parameters

Recruiting
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Record status
This record was last updated September 25, 2024 (before its estimated September 30, 2024 completion). Its status may not reflect the trial's current state.
Summary
In this study, among the patients who applied to the Physical Medicine and Rehabilitation outpatient clinic of Muğla Training and Research Hospital and were diagnosed with subacromial impingement by anamnesis and clinical tests, inclusion criteria) and exclusion criteria will be included in the study. Demographic data of the patients will then be recorded. DASH (Disabilities of the Arm, Shoulder and Hand) and Constant Murley scores will be calculated. 4 years of musculoskeletal ultrasound experience will be recorded by a radiologist using ultrasound (Siemens® V8, LA2-14A probe) in modified Crass position (positioning with the palm of the examined side on the posterior iliac wing) by measuring subacromial bursa thickness, supraspinatus tendon thickness, acromiohumeral distance, supraspinatus tendon thickness/acromiohumeral distance ratio. Demographic data of the patients will then be recorded. DASH (Disabilities of the Arm, Shoulder and Hand) and Constant Murley scores will be calculated.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2024-04-22; most recent amendment 2024-09-23.
Trial Details
NCT Number NCT06384430
Lead Sponsor Muğla Sıtkı Koçman University
Conditions Subacromial Impingement Syndrome, Shoulder Tendinitis, Shoulder Bursitis, Shoulder Pain
Enrollment 70 participants
Start Date 2024-04-01
Primary Completion 2024-09-30 (estimated)
Study Completion 2024-10-31 (estimated)
Updated on ClinicalTrials.gov 2024-09-25