Subacromial Impingement Syndrome Functional Tests Correlation With Ultrasound Parameters
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-70
SponsorMuğla Sıtkı Koçman University
About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Being between 18-70 years old
Clinical evaluation positive for subacromial impingement syndrome (Neer's test, Hawkins Kennedy, supraspinatus palpation test)
Disqualifiers
Under 18, over 70 years of age
Those diagnosed with rheumatologic diseases
Those with symptomatic shoulder osteoarthritis
Those with shoulder instability
Trial population
Being between 18-70 years old and clinical evaluation positive for subacromial impingement syndrome.
Trial design
Design model
Cohort
Time perspective
Cross-sectional
Treatments tested in this trial
Shoulder functional tests and ultrasound
Diagnostic testOn the day of the study, demographic data will be collected from patients with a clinical diagnosis of impingement and who agree to participate in the study, then DASH and Constant Murley scores will be calculated and subacromial bursa thickness, supraspinatus tendon thickness, acromiohumeral distance, supraspinatus tendon thickness/acromiohumeral distance ratio will be calculated on ultrasound.
Treatment groups
70 Participants
are divided into 1 treatment groupGroup A: Patients with subacromial impingement syndrome1 intervention
Trial outcomes
Primary outcomes
1
subacromial bursa thickness
subacromial bursa thickness measure
Time frame
1 day2
supraspinatus tendon thickness
supraspinatus tendon thickness measure
Time frame
1 day3
acromiohumeral distance
acromiohumeral distance measure
Time frame
1 daySponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov