Clinical and Radiological Results of Total Hip Arthroplasty Using a Ceramic Friction Pair (CERAM)

Stryker Trauma and Extremities

Status: Completed

Conditions: Congenital Dislocations; Primary, Secondary or Post-traumatic Osteoarthrosis; Hip Replacement; Femur Head Necrosis

Study type: Observational

Funder types: Industry

Identifiers

NCT02062437

1301-T-CERAM-R

Details and patient eligibility

About

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.

Enrollment: 132 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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.

Exclusion criteria

• Patient having a tumoral pathology.
• Patient having expressed opposition to the study participation.

Trial design

132 participants in 1 patient group

Total hip replacement using a ceramic friction pair

Description:

Patients treated with total hip replacement using a ceramic friction pair Biolox® Delta, with Meije Duo® stem associated with Dynacup® cup