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Total Knee Arthroplasty With Vitamin E Polyethylene

NCT05810285 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 186

Last updated 2025-01-03

Study results available
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Summary

The aim of this observational study is to investigate if there is any difference in survival rate, clinical and radiological results after total knee replacement with vitamin E-blended polyethylene in comparison to conventional polyethylene at minimum 7-year follow-up

Conditions

Interventions

DEVICE

GKS Prime Flex Mobile knee

Total knee arthroplasty with a cemented mobile bearing bicompartmental knee prosthesis

Sponsors & Collaborators

  • Permedica spa

    lead INDUSTRY

Principal Investigators

  • Marco Spezia, MD · Ospedale Centro Ortopedico di Quadrante

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-04-12
Primary Completion
2023-06-27
Completion
2023-06-27

Countries

  • Italy

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05810285 on ClinicalTrials.gov