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Recruiting NCT06838247

NCT06838247 Ultrasonographic Analysis of Post-Traumatic Shoulder Lesions After Hand Trauma

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Clinical Trial Summary
NCT ID NCT06838247
Status Recruiting
Phase
Sponsor Ankara Training and Research Hospital
Condition Shoulder
Study Type OBSERVATIONAL
Enrollment 60 participants
Start Date 2024-11-11
Primary Completion 2026-06-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 65 Years
Study Type OBSERVATIONAL

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 60 participants in total. It began in 2024-11-11 with a primary completion date of 2026-06-01.

⚠ 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

The purpose of the study is to reveal whether there are concurrent shoulder lesions in patients with hand injuries. Its importance is that it will shed light on whether not only the hand but also the shoulder should be included in the treatment program in hand rehabilitation.

Eligibility Criteria

Inclusion Criteria: * Having a history of hand injury and applying for hand rehabilitation after surgical and conservative treatment. Exclusion Criteria: * Being under 18 and over 65 years of age * Patients with systemic diseases (Diabetes mellitus, Peripheral vascular diseases) * Any rheumatic disease involving the hand and upper extremity * History of neuropathy involving the hand and upper extremity * Those with any shoulder problems prior to the hand injury * Those with an open wound on the hand * Those who cannot cooperate * Other upper extremity traumatic injuries occurring during the hand injury

Contact & Investigator

Central Contact

Nadide Koca, M.D.

✉ nadide.koca@gmail.com

📞 +905376843434

Frequently Asked Questions

Who can join the NCT06838247 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Shoulder. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06838247 currently recruiting?

Yes, NCT06838247 is actively recruiting participants. Contact the research team at nadide.koca@gmail.com for enrollment information.

Where is the NCT06838247 trial being conducted?

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

Who is sponsoring the NCT06838247 clinical trial?

NCT06838247 is sponsored by Ankara Training and Research Hospital. The trial plans to enroll 60 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology