Subacromial Impingement Syndrome Functional Tests Correlation With Ultrasound Parameters

StatusUnknown
PhaseNot specified
Started

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.

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Record History

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  1. Minor Changed Registry marked status Unknown (sponsor has not verified the record since Sep 2024); last known: Recruiting
  2. Minor Primary completion date: Aug 31, 2024 to Sep 30, 2024
    • Study completion date: Sep 1, 2024 to Oct 31, 2024
    v3
  3. Minor Study description expanded, about 242 words
    • Study title expanded, about 6 words
    v2
  4. Minor Study First Submitted
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT06384430
Lead Sponsor Muğla Sıtkı Koçman University
Conditions
(from sponsor)
Subacromial Impingement Syndrome, Shoulder Tendinitis, Shoulder Bursitis, Shoulder Pain
Related terms Shoulder Impingement Syndrome, Shoulder Pain
Enrollment 70 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov