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Recruiting NCT07440251

NCT07440251 Evaluation of Dual Fixation of Distal Ulna Fractures by Flexible Intramedullary Nail and Mini Locked Plate 2.7 mm.

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Clinical Trial Summary
NCT ID NCT07440251
Status Recruiting
Phase
Sponsor Sohag University
Condition Distal Ulna Fracture
Study Type INTERVENTIONAL
Enrollment 18 participants
Start Date 2026-02-20
Primary Completion 2026-08

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Dual fixation of distal ulna fractures by flexible intramedullary nail and mini locked plate 2.7 mm

Eligibility Fast-Check

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

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 18 participants in total. It began in 2026-02-20 with a primary completion date of 2026-08.

⚠ 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

Although isolated fixation methods, such as intramedullary nails or plate fixation, are commonly employed, certain fracture patterns-particularly comminuted, osteoporotic, or unstable fractures- represent a challenge to achieve stable fixation and restoring normal anatomy . Dual fixation, combining an intramedullary nail with a low-profile 2.7-mm mini locked plate, aims to capitalize on the strengths of both techniques-a concept known as "orthogonal or hybrid stabilization". This combined approach provides enhanced biomechanical stability, allows for early mobilization by sharing the mechanical load, and minimizes the risk of non-union or hardware failure. Studying the clinical and radiological outcomes of this dual fixation strategy is essential to establish its efficacy and safety in managing complex distal ulna fractures.

Eligibility Criteria

Inclusion Criteria: * Displaced distal ulna fractures either isolated or with associated distal radius fractures. * Unstable distal ulna fractures * Age group: \[Adults aged 18 years and older\]. Exclusion Criteria: * Open fractures with severe soft tissue injury (Gustilo type III). * Pathological fractures. * Patients with systemic conditions affecting bone healing e.g. uncontrolled diabetes and severe osteoporosis.

Contact & Investigator

Central Contact

Mostafa Ali Hamed

✉ mostafaalihamed97@gmail.com

📞 +201006850240

Frequently Asked Questions

Who can join the NCT07440251 clinical trial?

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

Is NCT07440251 currently recruiting?

Yes, NCT07440251 is actively recruiting participants. Contact the research team at mostafaalihamed97@gmail.com for enrollment information.

Where is the NCT07440251 trial being conducted?

This trial is being conducted at Sohag, Egypt.

Who is sponsoring the NCT07440251 clinical trial?

NCT07440251 is sponsored by Sohag University. The trial plans to enroll 18 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