Clinical and Radiographic Outcomes of the JointMedica Polymotion Resurfacing (PHR) Device

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age21+
SponsorJointMedica Inc.

About this trial

The goal of this observational study is to generate Real World Evidence (RWE) on the device performance of the Polymotion Hip Resurfacing (PHR) system and its use in patients who have been implanted with the device for the treatment of hip osteoarthritis.

This study will assess the following endpoints:

* The survivorship of the Acetabular Cup (Kaplan-Meier estimate) through 2 years of follow-up. * Radiographic success of the implanted cups, through quantitative motion analysis to assess migration of the acetabular cups. * Absence of subsequent surgical intervention at the acetabulum of there operated hip. * Absence of serious, device-related adverse events. * Patient reported outcomes through Harris Hip Score and SUSHI - UCLA Hip Score questionnaires.

Eligibility criteria

Qualifiers

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

Disqualifiers

There is no exclusion criteria for this study

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

105 Participants
are grouped into 1 trial group

Sponsors and collaborators