Polyethylene Wear Particle Analysis of THA

Description

Purpose of research The purpose of this study was to demonstrate that polyethylene (Vitamin E-containing polyethylene), a newly introduced biomaterial for tibial inserts in hip replacement surgery and widely used clinically, but whose mid- to long-term clinical results are still unknown, is superior to conventional polyethylene in vivo. The aim of this project is to conduct an international multi-center joint research study to determine whether polyethylene wear debris production can be reduced in the future, using an in vivo polyethylene wear debris analysis method that the investigators developed as a method that can provide early feedback.

Conditions

Wear of Articular Bearing Surface of Prosthetic Joint, Hip Arthropathy

Study Overview

Study Details

Study overview

Purpose of research The purpose of this study was to demonstrate that polyethylene (Vitamin E-containing polyethylene), a newly introduced biomaterial for tibial inserts in hip replacement surgery and widely used clinically, but whose mid- to long-term clinical results are still unknown, is superior to conventional polyethylene in vivo. The aim of this project is to conduct an international multi-center joint research study to determine whether polyethylene wear debris production can be reduced in the future, using an in vivo polyethylene wear debris analysis method that the investigators developed as a method that can provide early feedback.

Polyethylene Wear Particle Analysis of Total Hip Arthroplasty -International Multicenter Study-

Polyethylene Wear Particle Analysis of THA

Condition
Wear of Articular Bearing Surface of Prosthetic Joint
Intervention / Treatment

-

Contacts and Locations

Rochester

Mayo Clinic, Rochester, Minnesota, United States, 55905

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Patients undergoing revision hip arthroplasty within the study period
  • 2. Patients over 20 years old
  • 3. Patients who have received a sufficient explanation, have sufficient understanding, and have given their free written consent.
  • 4. Patients who have passed 2 years or more since their first total hip arthroplasty
  • 1. Patients who are judged to be unsuitable as research subjects by the research physician

Ages Eligible for Study

20 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Osaka Metropolitan University,

Yukihide Minoda, MD, PhD, PRINCIPAL_INVESTIGATOR, Osaka Metropolitan University

Study Record Dates

2028-12-31