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Clinical Trials/NCT04501185
NCT04501185
Recruiting
N/A

Comparison of Clinical Results of Two Cementless Femoral Stem

Chang Gung Memorial Hospital1 site in 1 country60 target enrollmentJune 1, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
Osteoarthritis, Hip
Sponsor
Chang Gung Memorial Hospital
Enrollment
60
Locations
1
Primary Endpoint
Numerical Rating Scale
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

In the present study, two types of cementless femoral stem- UTS Stem and UTF-reduced Stem- were utilized in total hip arthroplasty. Due to the design for proximal femur fixation, both femoral stems could prevent stress shielding around the implant, further preventing osteolysis. The difference between both femoral stems is the length, in which UTS Stem is 20% shorter than UTF-reduced Stem. The clinical outcomes of both femoral stems will be compared. Both femoral stems are expected to have equally good radiologic outcome and clinical performance.

Detailed Description

Total hip arthroplasty (THA) is a common orthopedic procedure aimed at improving joint function and alleviating pain in patients with hip joint degeneration. However, the phenomenon of stress shielding-whereby the mechanical properties of the prosthesis lead to reduced load transmission to the surrounding bone-can compromise long-term outcomes. In particular, uncemented THA designs are susceptible to stress shielding, potentially resulting in bone resorption and implant loosening. To address this challenge, the study focuses on optimizing femoral stem fixation within the proximal femur in two specific stem designs: the UTS and the UTF reduced stem. These stems are strategically designed to enhance load transfer while minimizing stress shielding effects. A total of 60 patients who are undergoing total hip arthroplasty at Linkou Chang Gung Memorial Hospital will be recruited, including 30 patients in the "UTS" group and 30 patients in the "UTF-reduced" group.The clinical assessments including Success Rate of prosthesis, Numerical Rating Scale (NRS) for pain, Harris Hip Score (HHS), Medical Outcome Study Short Form-36 (SF-36) and : Dual-energy X-ray absorptiometry (DEXA) scanning for bone mineral density monitoring.

Registry
clinicaltrials.gov
Start Date
June 1, 2020
End Date
May 2026
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Chang Gung Memorial Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients who receive total hip arthroplasty with either a UTS femoral stem or a UTF-reduced femoral stem after June, 2020
  • Patients who have not received total hip arthroplasty in the past

Exclusion Criteria

  • Patients who are unable or unwilling to return for follow-up
  • Patients who suffer from mental disorders

Outcomes

Primary Outcomes

Numerical Rating Scale

Time Frame: Change from baseline at 1 year

Numerical Rating Scale is a patient-reported outcome measure. The scale ranges from 0 to 10. A score of 0 represents no pain, while a score of 10 represents extreme pain.

Harris Hip Score

Time Frame: Change from baseline at 1 year

Harris Hip Score includes 4 sections that evaluate pain, function, deformity, and range of motion. Total scores is from 0 to 100, higher scores represent a better outcome.

DEXA scanning

Time Frame: Change from baseline at 1 year

DEXA scanning is used to monitor and quantify bone mineral density, which helps to understand if the implant has an effect on the change of bone mineral density.

Success rate

Time Frame: Duration of 1 year

Failure is defined as removal or revision of any components as a result of mechanical failure or complications. Sucess is defined as implants that are sucessfully implanted without any failure for the duration of 1 year. The success rate will be represented as a percentage (%).

Medical Outcome Study Short Form-36

Time Frame: Change from baseline at 1 year

SF-36 is a set of generic, coherent, and easily administered quality-of-life measures. These measures rely upon patient self-reporting and are now widely utilized by managed care organizations and by Medicare for routine monitoring and assessment of care outcomes in adult patients. It consists of two sections, physical component summary and mental component summary, with 36 items in total.

Secondary Outcomes

  • Radiolucent line(Change from baseline at 1 year)
  • Morphology of the proximal femur(at baseline)
  • Valgus/Varus alignment(Change from baseline at 1 year)

Study Sites (1)

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