Recruiting soon

JointMedica Polymotion Resurfacing Device Outcomes for Hip Patients

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What is being collected

Data Collection

Who is being recruted

Over 21 Years
See all eligibility criteria
How is the trial designed

Case-Only

Examining characteristics of individuals with a disease in order to identify genetic or environmental factors contributing to the condition.
Observational
Study Start: July 2025
See protocol details

Summary

Principal SponsorJointMedica Inc.
Study ContactSteve MeakinsMore contacts
Last updated: December 11, 2025
Sourced from a government-validated database.Claim as a partner

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.

Official TitleClinical and Radiographic Outcomes of the JointMedica Polymotion Resurfacing (PHR) Device 
Principal SponsorJointMedica Inc.
Study ContactSteve MeakinsMore contacts
Last updated: December 11, 2025
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

105 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-only

These studies focus only on individuals who have a specific disease. Researchers examine patterns—often genetic or environmental—to uncover what might be linked to the condition.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

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

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

Suspended

Mark Rickman

Adelaide, AustraliaSee the location
Suspended

Gateway Surgery Centre

Calgary, Canada
Suspended

Orthopaedic Specialist Centre

Auckland, New Zealand
Recruiting soon3 Study Centers