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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05996510
Other study ID # BursaYIEAH
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 10, 2023
Est. completion date October 11, 2023

Study information

Verified date May 2024
Source Bursa Yüksek Ihtisas Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Chronic shoulder pain is one of the most common diseases affecting the quality of life today. Although there are multiple causes, one of the most common causes is shoulder impingement syndrome. Ultrasound can be used for diagnosis in patients whose treatment is difficult due to its complex structure. While the supraspinatus muscle, tendon and shoulder joint are the regions that are usually evaluated, the visualization of the Suprascapular notch is usually observed during injection. The connection between the suprascapular notch and the shoulder joint has been demonstrated in different studies.


Description:

In this study, the investigation of the relationship between the measurements of the suprascapular nerve and the suprascapular notch, which the investigators observed in our clinical ultrasound applications, and the disease activity intended.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date October 11, 2023
Est. primary completion date October 10, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - chronic shoulder pain - 35-65 years - who agreed to participate in the study Exclusion Criteria: - . Lymphoproliferative diseases and other neoplasms - .Uncontrolled arterial hypertension - Metabolic syndrome - Uncontrolled diabetes mellitus - Mental retardation - Antidepressant use - Autoimmune diseases

Study Design


Related Conditions & MeSH terms


Intervention

Device:
ultrasound
Shoulder ultrasound is performed using a linear ultrasound probe. The area under the suprascapular notch and the superior transverse scapular ligament is measured using the cross-sectional area measurement method.

Locations

Country Name City State
Turkey Bursa Yüksek Ihtisas Egitim ve Arastirma Hastanesi Bursa

Sponsors (1)

Lead Sponsor Collaborator
Bursa Yüksek Ihtisas Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Suprascapular notch cross-sectional area measurement The area under the suprascapular notch and the superior transverse scapular ligament is measured using the cross-sectional area measurement method. baseline
Secondary Visual Analogue Scale Visual Analog Scale was used for pain. Pain intensity was measured using 0-10 cm visual analogue scale (VAS). The findings suggested that 100-mm VAS ratings of 0 to 4 mm can be considered no pain; 5 to 44 mm, mild pain; 45 to 74 mm, moderate pain; and 75 to 100 mm, severe pain. baseline
Secondary Shoulder Pain and Disability Index (SPADI) The Shoulder Pain and Disability Index (SPADI) is a patient completed questionnaire with 13 items assessing pain level and extent of difficulty with activity of daily livings requiring the use of the upper extremities. The pain subscale has 5-items and the Disability subscale has 8-items.To score either version of the SPADI, the total score is calculated by averaging the pain and disability subscale scores to find a score out of 100. On this scale, 0 represents less disability while 100 represents greatest disability baseline
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