Multicentric Observational Study Evaluating Clinical and Radiological Results of a Total Hip Arthroplasty Using a Ceramic Friction Pair

Stryker Trauma and Extremities0 sites132 target enrollmentSeptember 2013

ConditionsHip Replacement Primary, Secondary or Post-traumatic Osteoarthrosis Femur Head Necrosis Congenital Dislocations

Overview

Phase: N/A
Intervention: Not specified
Conditions: Hip Replacement
Sponsor: Stryker Trauma and Extremities
Enrollment: 132
Primary Endpoint: Number of Participants With Adverse Events
Status: Completed
Last Updated: 8 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

The aim of this study is to assess safety and general performance of total hip arthroplasty, composed of a Meije Duo® femoral stem associated with a Dynacup® cup, and using the friction pair Biolox® Delta Ceramic.

Registry

clinicaltrials.gov

Start Date

September 2013

End Date

January 2014

Last Updated

8 years ago

Study Type

Observational

Sex

All

Investigators

Sponsor

Stryker Trauma and Extremities

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•Male or female patient implanted with a primary total hip replacement using a ceramic friction pair including Meije Duo® stem associated with a Dynacup® cup.
•Aged of more than 18 years at the time of the surgery.
•Patient with a follow-up of at least 2 years after surgery based on a consecutive and exhaustive series of patients operated within the inclusion period.
•Able to understand information to participate to the study.