Subacromial Impingement Syndrome Functional Tests Correlation With Ultrasound Parameters
NCT ID: NCT06384430
Last Updated: 2024-09-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
70 participants
OBSERVATIONAL
2024-04-01
2024-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Ultrasonographic Analysis of Post-Traumatic Shoulder Lesions After Hand Trauma
NCT06838247
Role of Dynamic Ultrasound in Assessment of Shoulder Impingement Syndrome
NCT06754592
Effectiveness of Supervised Exercise Program in Subacromial Impingement Syndrome
NCT04186624
the Thickness of the Muscles and Pain in Impingement Syndrome
NCT06665139
The Relationship of Critical Shoulder Angle With Proprioception and Disability
NCT06878846
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
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)
Shoulder functional tests and ultrasound
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.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Shoulder functional tests and ultrasound
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.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Clinical evaluation positive for subacromial impingement syndrome (Neer's test, Hawkins Kennedy, supraspinatus palpation test)
Exclusion Criteria
2. Those diagnosed with rheumatologic diseases
3. Those with symptomatic shoulder osteoarthritis
4. Those with shoulder instability
5. Shoulder pain in active, passive cervical spine movements
6. Previous shoulder surgery
7. 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)
8. Physiotherapy or intra-articular injection in the last 3 months
9. Diagnosis of type 2 diabetes or hypothyroidism
18 Years
70 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Muğla Sıtkı Koçman University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Nihal KARAYER OZGUL
Principal Investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Mugla Egitim Arastima
Muğla, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Nihal KARAYER OZGUL, 1
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
MuğlaSKU-NKO
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.