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Recruiting NCT07409818

NCT07409818 A Novel Classification in Calcific Tendinitis of the Shoulder: Evaluating MRI Localization and Related Treatment Strategies

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Clinical Trial Summary
NCT ID NCT07409818
Status Recruiting
Phase
Sponsor Koç University
Condition Calcific Tendinitis of Shoulder
Study Type OBSERVATIONAL
Enrollment 400 participants
Start Date 2025-10-02
Primary Completion 2026-10-01

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Conservative non-surgical treatmentDebridementSide to side repair

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 400 participants in total. It began in 2025-10-02 with a primary completion date of 2026-10-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Calcific tendinitis of the shoulder is among the frequently encountered shoulder problems. Conservative treatment is often preferred for its management. Persistent pain, impingement symptoms due to large calcific deposits, and extension into the bone are indications for surgical intervention. Although many classification methods for calcific tendinitis have been defined in the literature, none of them is directly related to prognosis, treatment options, or surgical management. The aim of this study is to create a new, easy-to-apply, practical, and treatment-related classification system for calcific tendinitis based on the localization of the deposits on MRI. Furthermore, the aim is to compile the current patient cohort according to this new classification and examine the relationship between the treatment applied and the deposit localization in the proposed classification.

Eligibility Criteria

Inclusion Criteria * Patients who underwent surgical treatment for calcific tendinitis * Presence of single or multiple calcific deposits within the rotator cuff tendons Exclusion Criteria * History of prior ipsilateral shoulder surgery for indications other than calcific tendinitis * Revision surgery for calcific tendinitis * Incomplete clinical documentation or unavailable MRI data

Contact & Investigator

Central Contact

Ata Cem Akbaba, Medical Doctor

✉ atacemakbaba1996@hotmail.com

📞 +905377397395

Principal Investigator

Mehmet S Demirhan, Medical Doctor

PRINCIPAL INVESTIGATOR

Koc University Hospital

Frequently Asked Questions

Who can join the NCT07409818 clinical trial?

This trial is open to participants of all sexes, studying Calcific Tendinitis of Shoulder. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07409818 currently recruiting?

Yes, NCT07409818 is actively recruiting participants. Contact the research team at atacemakbaba1996@hotmail.com for enrollment information.

Where is the NCT07409818 trial being conducted?

This trial is being conducted at Istanbul, Turkey (Türkiye).

Who is sponsoring the NCT07409818 clinical trial?

NCT07409818 is sponsored by Koç University. The principal investigator is Mehmet S Demirhan, Medical Doctor at Koc University Hospital. The trial plans to enroll 400 participants.

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