None listed
Conditions
Brief summary
This randomised controlled trial aims to determine whether a total hip replacement with a larger 36 mm diameter prosthetic femoral head significantly reduces the incidence of dislocation one year following total hip replacement, compared to total hip replacement with a standard 28 mm diameter prosthetic femoral head. The effect of the larger femoral head on both polyethylene wear and acetabular cup migration is also being assessed.
Interventions
Total hip replacement using a 36 mm metal on highly cross-linked polyethylene articulation. This is a surgical procedure where the femoral head is removed and replaced by a metal prosthetic femoral head (which in this situation has a diameter of 36 mm), which is attached to a femoral stem inserted into the femur. The head then articulates with a plastic (highly cross-linked polyethylene) liner in a metal acetabular shell, which is inserted into the acetabulum. The duration of the operation is between about 45 minutes and 4 hours, depending on the complexity of the operation.
Sponsors
Study design
Eligibility
Inclusion criteria
undergoing primary total hip replacement involving a metal on polyethylene articulation, through a posterior surgical approach, for osteoarthritis, rheumatoid or other inflammatory arthritis, or previous fracture/dislocation/surgery to the hip; or undergoing revision total hip replacement (involving a metal on polyethylene articulation) of a hemiarthroplasty or revision of a total hip replacement
Exclusion criteria
age <60 years (revisions: <50), neuromuscular disease, abnormal abductor mechanism, abnormal acetabulum (primaries only), revision for instability or infection (revisions only)