Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07440251

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

Led by Sohag University · Updated on 2026-04-24

18

Participants Needed

1

Research Sites

27 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Displaced distal ulna fractures either isolated or with associated distal radius fractures.
  • Unstable distal ulna fractures
  • Adults aged 18 years and older.
Not Eligible

You will not qualify if you...

  • 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.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Faculty of medicine sohag university

Sohag, Egypt

Actively Recruiting

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Research Team

M

Mostafa Ali Hamed

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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