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ID07409818

A Novel Classification in Calcific Tendinitis of the Shoulder: Evaluating MRI Localization and Related Treatment Strategies

Led by Koç University · Updated on 2026-02-13

400

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Calcific tendinitis of the shoulder is a common condition involving calcium deposits in the rotator cuff tendons, often causing pain and functional issues. While many classification systems exist, they do not directly guide treatment or prognosis. This study aims to create a new, practical classification based on MRI localization of the deposits, and to explore how this classification relates to the treatments patients receive. The study reviews MRI scans and clinical records from patients treated for calcific tendinitis between 2004 and 2025. Patients are categorized into five groups according to where the calcium deposits are located on MRI: outside the tendon, inside near the joint side, inside near the bursal side, completely within the tendon, or extending into the bone. Treatments include conservative non-surgical methods like pain relief and rest, or surgical interventions such as removal of the deposit and tendon repair techniques. Participants' medical records, operative notes, and treatment details are examined to see how treatment relates to the new classification. The main outcome measured is the change in shoulder function and pain scores from before treatment to 12 months after surgery. This observational study involves reviewing existing patient data to understand the link between deposit location and treatment outcomes over time.

CONDITIONS

Brief Title

A Novel Classification in Calcific Tendinitis of the Shoulder: Evaluating MRI Localization and Related Treatment Strategies

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients who underwent surgical treatment for calcific tendinitis
  • Presence of single or multiple calcific deposits within the rotator cuff tendons
Not Eligible

You will not qualify if you...

  • History of prior ipsilateral shoulder surgery for indications other than calcific tendinitis
  • Revision surgery for calcific tendinitis
  • Incomplete clinical documentation or unavailable MRI data

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Varies based on scheduling and imaging availability

Participants undergo MRI scans to determine the location and classification of calcific deposits in the shoulder.

1 visit (in-person) for MRI scan

Observation of Treatment

Duration - Varies per individual treatment plan

Participants receive either conservative non-surgical treatment or surgical interventions such as debridement, side to side repair, or anchor fixation based on clinical evaluation and MRI classification.

Visits depend on treatment modality; may include surgical and follow-up visits or conservative management visits

Long-term Monitoring

Duration - Up to 12 months

Participants are monitored for changes in shoulder function and symptoms up to 12 months post-treatment to assess outcomes.

Follow-up visits for assessment up to 12 months post-treatment

Trial Site Locations

Total: 1 location

1

Koç University Hospital

Istanbul, Zeytinburnu, Turkey (Türkiye), 34010

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Research Team

A

Ata Cem Akbaba, Medical Doctor

İ

İlker Eren, Medical Doctor

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

5

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Published Research Related To This Trial

Intraosseous calcific tendinitis of the rotator cuff yields similar outcomes to those of intratendinous lesions despite worse preoperative scores.

Emrah Caliskan, Ilker Eren, Lercan Aslan...

https://pubmed.ncbi.nlm.nih.gov/35044474