JointMedica Polymotion Resurfacing Device Outcomes for Hip Patients
Data Collection
Case-Only
Examining characteristics of individuals with a disease in order to identify genetic or environmental factors contributing to the condition.Summary
Study start date: July 25, 2025
Actual date on which the first participant was enrolled.This study aims to evaluate the performance and safety of a hip implant device known as the JointMedica Polymotion Hip Resurfacing (PHR) device. It focuses on individuals who have already received this implant in Canada, New Zealand, and Australia. Up to 70 patients will be involved in this research to understand how well the implant is functioning over time. The study is important because it helps determine the durability and effectiveness of the implant, ensuring that it meets the needs of patients who rely on it for improved mobility and reduced pain. Participants will be asked to attend a follow-up visit as part of their standard care routine. During these visits, doctors will collect clinical data by conducting an x-ray of the hip and asking patients to fill out two questionnaires about their hip function and overall outcomes. The information collected, including the x-ray images, will be analyzed to see how well the implant is holding up, particularly the acetabular cup, which is a part of the hip joint. Researchers will look for any issues that might require additional surgery and monitor for any serious side effects related to the implant. This helps ensure that the device continues to be a safe and effective treatment option for patients.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.105 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Case-only
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 21 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Inclusion Criteria: * Age 21 or above at the time of the surgery. * Have had the Polymotion Hip Resurfacing (PHR) (implanted between September 2020 to January 2025 * Written informed consent given by subject Exclusion Criteria: * There is no exclusion criteria for this study
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 3 locations
Gateway Surgery Centre
Calgary, CanadaOrthopaedic Specialist Centre
Auckland, New Zealand