RECRUITING

Polyethylene Wear Particle Analysis of THA

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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.

Official Title

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

Quick Facts

Study Start:2024-06-01
Study Completion:2028-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06432543

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.

Ages Eligible for Study:20 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Patients undergoing revision hip arthroplasty within the study period
  2. 2. Patients over 20 years old
  3. 3. Patients who have received a sufficient explanation, have sufficient understanding, and have given their free written consent.
  4. 4. Patients who have passed 2 years or more since their first total hip arthroplasty
  1. 1. Patients who are judged to be unsuitable as research subjects by the research physician

Contacts and Locations

Study Contact

Kiyoko Kato, MD
CONTACT
81-6-6645-3851
Kiyoko-Kato@omu.ac.jp

Principal Investigator

Yukihide Minoda, MD, PhD
PRINCIPAL_INVESTIGATOR
Osaka Metropolitan University

Study Locations (Sites)

Mayo Clinic
Rochester, Minnesota, 55905
United States

Collaborators and Investigators

Sponsor: Osaka Metropolitan University

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

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-06-01
Study Completion Date2028-12-31

Study Record Updates

Study Start Date2024-06-01
Study Completion Date2028-12-31

Terms related to this study

Keywords Provided by Researchers

  • Polyethylene wear particle
  • Total hip arthroplasty

Additional Relevant MeSH Terms

  • Wear of Articular Bearing Surface of Prosthetic Joint
  • Hip Arthropathy