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Recruiting NCT06531590

NCT06531590 Anterior Shoulder Dislocation at Emergency Department

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Clinical Trial Summary
NCT ID NCT06531590
Status Recruiting
Phase
Sponsor Saglik Bilimleri Universitesi
Condition Shoulder Dislocation
Study Type OBSERVATIONAL
Enrollment 140 participants
Start Date 2024-03-01
Primary Completion 2026-03-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

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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 140 participants in total. It began in 2024-03-01 with a primary completion date of 2026-03-01.

⚠ 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

In this study, investigator will analyze the demographic characteristics of patients presenting to emergency department with Anterior Shoulder Dislocation. Investigators will document the mechanism of injury, orthopedic classification of shoulder dislocation, associated treatments, pre-procedural pain scoring, post-procedural pain scoring, as well as the duration of emergency department stay related to the preferred treatment, orthopedic consultation, and patient outcomes (discharge, admission to ward or intensive care unit, mortality). Aim of the study to investigate whether the current treatments used provide any superiority in emergency department outcomes for patients

Eligibility Criteria

Inclusion Criteria: Patients aged 18 years and older Exclusion Criteria: Patients who are not conscious at the time of admission and do not consent to participate in the study. Patients who do not have follow-up in our healthcare system or cannot be followed up. Patients with allergies to opioids or local anesthetics. Patients presenting to the emergency department with suspicion of multiple fractures and dislocations involving ≥2 different types of injuries will also be excluded from the study. Forensic cases

Contact & Investigator

Central Contact

gulsen akcay, ass. prof.

✉ gulakcay@yahoo.com.tr

📞 +905052874949

Principal Investigator

gulsen akcay, ass. prof.

STUDY DIRECTOR

ass. prof. of organization

Frequently Asked Questions

Who can join the NCT06531590 clinical trial?

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

Is NCT06531590 currently recruiting?

Yes, NCT06531590 is actively recruiting participants. Contact the research team at gulakcay@yahoo.com.tr for enrollment information.

Where is the NCT06531590 trial being conducted?

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

Who is sponsoring the NCT06531590 clinical trial?

NCT06531590 is sponsored by Saglik Bilimleri Universitesi. The principal investigator is gulsen akcay, ass. prof. at ass. prof. of organization. The trial plans to enroll 140 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: July 2026  ·  Data Methodology