Status:
COMPLETED
Comparison of the Efficiency of Ultrasound-Guided Lavage and Subacromial Bursa Injection in Calcific Tendinitis
Lead Sponsor:
Istanbul University - Cerrahpasa
Conditions:
Calcific Tendinitis
Calcific Tendinitis of Shoulder
Eligibility:
All Genders
18-75 years
Phase:
NA
Brief Summary
It is aimed to compare in the early period the clinical and ultrasonographic findings in terms of the effectiveness of ultrasound-guided subacromial bursa injection with corticosteroid and ultrasound-...
Detailed Description
Calcific tendinitis is a disease that occurs with the precipitation of hydroxyapatite crystals on tendons and shoulder region is the most involved. In the shoulder region, calcific tendinitis can invo...
Eligibility Criteria
Inclusion
- Cases diagnosed with calcific tendinitis who did not benefit from conservative treatment
- Cases with calcific deposits greater than 1 cm in direct radiography, ultrasonography, or magnetic resonance imaging
- Cases between the ages of 18-75 whose informed consent was obtained for participation in the study
Exclusion
- Cases with radiculopathy ipsilateral to the affected shoulder
- Cases with active inflammatory arthropathy of the affected shoulder
- Cases with previous shoulder surgery
- Cases with a history of humeral head, scapula, and clavicle fractures
- Cases with neurological deficit affecting the upper extremity
- Cases with uncontrolled diabetes mellitus and uncontrolled hypertension, uncompensated congestive heart failure, chronic renal failure, chronic liver disease, tumor and/or vascular disease, inflammatory and/or infectious diseases, currently active psychiatric disease
- Cases with a history of subacromial bursa injection, calcific lavage or shoulder joint injection in the last 3 months
- Cases with a history of allergic reaction to the substance to be applied as local anesthetic
- Pregnancy or lactation
- Anticoagulant or antiagregant (antiplatelet) medication use that may interfere with the injection procedure.
Key Trial Info
Start Date :
March 9 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 30 2022
Estimated Enrollment :
32 Patients enrolled
Trial Details
Trial ID
NCT05272085
Start Date
March 9 2022
End Date
November 30 2022
Last Update
January 31 2023
Active Locations (1)
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1
Istanbul University- Cerrahpaşa
Istanbul, Turkey (Türkiye), 34098