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Highly Cross-linked Polyethylene in Total Knee Arthroplasty

NCT03622398 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 125

Last updated 2019-07-23

No results posted yet for this study

Summary

The aim of this study was to determine clinical and radiographic results after posterior cruciate-substituting total knee arthroplasties with highly cross-linked polyethylene in one knee and compression mold conventional polyethylene in the contralateral knee in the same patients.

Conditions

  • Knee Arthroplasty, Total

Interventions

PROCEDURE

Total knee arthroplasty with HXLPE liner

Replacing arthritic knee with a metal device, and using a highly cross-linked polyethylene(HXLPE) liner in between metallic surfaces.

PROCEDURE

Total knee arthroplasty with conventional polyethylene liner

Replacing arthritic knee with a metal device, and using a conventional polyethylene liner in between metallic surfaces.

Sponsors & Collaborators

  • Ewha Womans University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-01-31
Primary Completion
2008-10-31
Completion
2018-06-30

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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 NCT03622398 on ClinicalTrials.gov