- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06384430
Subacromial Impingement Syndrome Functional Tests Correlation With Ultrasound Parameters
September 23, 2024 updated by: Nihal KARAYER OZGUL, Muğla Sıtkı Koçman University
Subacromial Impingement Syndrome: The Relationship Between Shoulder Functional Tests and Ultrasound Parameters
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.
Study Overview
Status
Recruiting
Intervention / Treatment
Detailed Description
Subacromial impingement syndrome is a common shoulder pain disorder.
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 (being between 18-70 years of age, positivity for subacromial impingement syndrome in clinical evaluation (Neer's test, Hawkins Kennedy, supraspinatus palpation test)) and exclusion criteria (under 18 years of age, over 70 years of age, rheumatologic disease diagnosis, symptomatic shoulder osteoarthritis, shoulder instability; shoulder pain in active, passive cervical spine movements, previous shoulder surgery, those with adhesive capsulitis findings (>50% passive range of motion restriction in 2 planes or full-thickness rotator cuff tear detected on ultrasound), those who received physiotherapy or intra-articular injections in the last 3 months, those with type 2 diabetes or hypothyroidism) 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.
Study Type
Observational
Enrollment (Estimated)
70
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Nihal KARAYER OZGUL, 1
- Phone Number: +905073068312
- Email: nihalkarayer505@gmail.com
Study Locations
-
-
-
Mugla, Turkey
- Recruiting
- Mugla Egitim Arastima
-
Contact:
- Nihal KARAYER OZGUL, 1
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
Being between 18-70 years old and clinical evaluation positive for subacromial impingement syndrome.
Description
Inclusion Criteria:
- Being between 18-70 years old
- Clinical evaluation positive for subacromial impingement syndrome (Neer's test, Hawkins Kennedy, supraspinatus palpation test)
Exclusion Criteria:
- Under 18, over 70 years of age
- Those diagnosed with rheumatologic diseases
- Those with symptomatic shoulder osteoarthritis
- Those with shoulder instability
- Shoulder pain in active, passive cervical spine movements
- Previous shoulder surgery
- Findings of adhesive capsulitis (>50% restriction of passive range of motion in 2 planes or detection of a full-thickness rotator cuff tear on ultrasound)
- Physiotherapy or intra-articular injection in the last 3 months
- Diagnosis of type 2 diabetes or hypothyroidism
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Patients with subacromial impingement syndrome
Patients with subacromial impingement syndrome: Being between 18-70 years old Clinical evaluation positive for subacromial impingement syndrome (Neer's test, Hawkins Kennedy, supraspinatus palpation test)
|
On 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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
subacromial bursa thickness
Time Frame: 1 day
|
subacromial bursa thickness measure
|
1 day
|
|
supraspinatus tendon thickness
Time Frame: 1 day
|
supraspinatus tendon thickness measure
|
1 day
|
|
acromiohumeral distance
Time Frame: 1 day
|
acromiohumeral distance measure
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 1, 2024
Primary Completion (Estimated)
September 30, 2024
Study Completion (Estimated)
October 31, 2024
Study Registration Dates
First Submitted
April 22, 2024
First Submitted That Met QC Criteria
April 22, 2024
First Posted (Actual)
April 25, 2024
Study Record Updates
Last Update Posted (Actual)
September 25, 2024
Last Update Submitted That Met QC Criteria
September 23, 2024
Last Verified
September 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MuğlaSKU-NKO
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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