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Comparison of the Efficiency of Ultrasound-Guided Lavage and Subacromial Bursa Injection in Calcific Tendinitis

I

Istanbul University - Cerrahpasa (IUC)

Status

Completed

Conditions

Shoulder Pain
Calcific Tendinitis
Calcific Tendinitis of Shoulder

Treatments

Procedure: Ultrasound Guided Subacromial Bursa Injection
Procedure: Ultrasound Guided Lavage

Study type

Interventional

Funder types

Other

Identifiers

NCT05272085
IstanbulUC-NTugbayYildiran-01

Details and patient eligibility

About

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-guided lavage, which are the treatment options available in the literature for patients with calcific tendinitis who do not respond to conservative treatment.

Full 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 involve all rotator cuff tendons, most commonly the supraspinatus. It may progress with pain and functional limitation. The pain can increase with movement or can occur at rest and sleep. The prevalence of calcific tendinitis is between 2.7% and 20% in the general population. The most common age group is between 30 and 60. It can negatively affect the family and social life of the person and cause loss of workforce.

Especially in the treatment of patients with calcific tendinitis unresponsive to conservative treatment, ultrasound-guided corticosteroid injection in subacromial bursa and ultrasound-guided lavage are frequently used treatment options. However, there are very few studies in the literature comparing these two treatment methods as randomized controlled trials.

In this study, it is aimed to compare the effectiveness of ultrasound guided subacromial bursa injection and ultrasound guided lavage procedures on pain scores, functional scales, disability scales, direct radiography findings and ultrasonographic imaging findings.

Enrollment

32 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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 criteria

  • 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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

32 participants in 2 patient groups

Ultrasound Guided Lavage Group
Active Comparator group
Description:
The physical examination, pain scoring, functional scale, disability scale, special tests, direct radiography findings and ultrasonographic imaging findings of the patients in this group before the treatment and 1 month after the treatment will be evaluated and will be recorded. Size of calcific deposits and Gartner classification will be evaluated on direct radiography. Size, shape, acoustic shadowing, power doppler activity of calcific deposits and other bursitis, tendinitis, ruptures, effusion in the shoulder will be evaluated on ultrasonographic imaging. Patients in this group will be treated with ultrasound-guided lavage.
Treatment:
Procedure: Ultrasound Guided Lavage
Ultrasound Guided Subacromial Bursa Injection Group
Active Comparator group
Description:
The physical examination, pain scoring, functional scale, disability scale, special tests, direct radiography findings and ultrasonographic imaging findings of the patients in this group before the treatment and 1 month after the treatment will be evaluated and will be recorded. Size of calcific deposits and Gartner classification will be evaluated on direct radiography. Size, shape, acoustic shadowing, power doppler activity of calcific deposits and other bursitis, tendinitis, ruptures, effusion in the shoulder will be evaluated on ultrasonographic imaging. Patients in this group will be treated with ultrasound-guided subacromial bursa injection with corticosteroid and lidocaine.
Treatment:
Procedure: Ultrasound Guided Subacromial Bursa Injection

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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