Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
NCT06449755

Elastic Nail Versus Screw for Intramedullary Fixation of Displaced Fractures of the Fifth Metacarpal Neck

Led by Istanbul University · Updated on 2024-06-10

46

Participants Needed

1

Research Sites

74 weeks

Total Duration

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AI-Summary

What this Trial Is About

The goal of this clinical trial is to compare two different intramedullary fixation technique in patient diagnosed with deplased fifth metacarpal neck fracture. The main questions it aims to answer are: * Can percutaneous screw application be a more stable fixation method than intramedullary elastic nail application? * Can screw application create a significant difference in the recovery of grip strength in the early period compared to elastic nail application? Patients will be followed up at the 1st week, 1st month and 3rd month postoperatively. Functionality will be evaluated with Quick DASH score at the 3rd month. At the 1st and 3rd month controls, grip strength will be evaluated. At the same time, metacarpal shortening and angulations will be measured on x-ray. Researchers will compare percutaneous screw and elastic nail group to see grip strength, healing time and radiologic parameter difference.

CONDITIONS

Official Title

Elastic Nail Versus Screw for Intramedullary Fixation of Displaced Fractures of the Fifth Metacarpal Neck

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18-60 years with displaced fifth metacarpal fractures with angulation greater than 30 degrees
Not Eligible

You will not qualify if you...

  • Open fracture
  • Patients with multiple injuries
  • History of hand surgery
  • Intraarticular metacarpal neck fractures

AI-Screening

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Trial Site Locations

Total: 1 location

1

Istanbul Unıversity Medicine Faculty Orthopaedic Department

Istanbul, Fatih, Turkey (Türkiye), 34080

Actively Recruiting

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Research Team

A

Ahmet Muçteba AM Yıldırım, Fellow

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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