Evaluation of radiographic and clinical outcomes following Absolut femoral prosthesis and Global acetabular cup total hip replacement surgery
Clinical and Radiological Outcome using the Absolut femoral prosthesis and the Global cup system following total hip arthroplasty in patients with Degenerative Joint Disease
Global Orthopaedic Technology Pty Ltd
150 participants
May 20, 2014
Interventional
Conditions
Summary
Fixation of the femoral stem and acetabular shell in their respective bones can be with cement, specialised coatings or a combination of the two (i.e. stem in cement, acetabulum with porous coating), known as hybrid fixation. The cemented Absolut hip stem with the non-cemented Global acetabular cup will be evaluated following primary total hip replacement surgery.
Eligibility
Inclusion Criteria1
- The individual is diagnosed with a primary diagnosis of Degenerative Joint Disease.
Exclusion Criteria3
- The individual has an active infection within the affected hip joint.
- The individual has had previous total hip replacement or hip fusion of the affected hip joint.
- The individual has a neuromuscular or neurosensory deficit which limits the ability to evaluate safety and effectiveness of the device or has a systemic disease that would affect the subject's welfare or overall outcome of the study.
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Interventions
Prospective study evaluating post-operative radiology and clinical outcomes in patients who undergo primary total hip replacement using the Absolut femoral stem and Global acetabular cup. Patients will be recruited over a 2 year period and followed up to 10 years after surgery. Duration of surgery will be as is standard for total hip arthroplasty.
Locations(3)
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ACTRN12614000318684