A Randomised Single Centre Study to Compare the Long-term Wear Characteristics of Marathon™ and Enduron™ Polyethylene Cup Liners in Primary Total Hip Replacement
- Conditions
- Congenital Hip DysplasiaTraumatic Femoral FracturesPost-traumatic ArthritisCollagen DisordersNonunion of Femoral FracturesOsteoarthritisAvascular NecrosisSlipped Capital Femoral Epiphysis
- Interventions
- Device: EnduronDevice: Marathon™
- Registration Number
- NCT00208442
- Lead Sponsor
- DePuy International
- Brief Summary
The purpose of this study is to compare the performance and compare the wear characteristics of two polyethylene cup liners, Marathon™ and Enduron™, in the treatment of patients with hip joint disease requiring a total hip replacement. Patients who enter the study will be randomly allocated to one of the polyethylene cup liners, Marathon™ or Enduron™ and will be evaluated at regular intervals using clinical and x-ray assessments.
- Detailed Description
The original protocol intended to perform clinical assessment using the Harris Hip Score, Merle D'Aubigne score and UCLA Activity Level Rating at 6 months, 1 year, 2 years, 3 years, 4 years, 5 years and 10 years post-operative. Merle D'Aubigne score evaluation was removed per Amendment 2.
However, protocol-specified data collected included only the linear and volumetric wear and incidence and pattern of radiological signs at 10 years post surgery. Data collected outside of the protocol included Oxford Hip Score and SF-12 for mental and physical well-being at 10 years post surgery and revision for any reason.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 122
i) Male or female subjects, aged between 45 and 75 years inclusive.
ii) Subjects who are able to give voluntary, written informed consent to participate in this investigation and from whom consent has been obtained.
iii) Subjects who, in the opinion of the Investigator, are able to understand this investigation, co-operate with the investigational procedures and are willing to return to the hospital for all the required post-operative follow-ups.
iv) Subjects with non-inflammatory arthritis of the hip who require a primary hip arthroplasty and are considered by the Clinical Investigator to be suitable for a cemented femoral component and an uncemented acetabular component.
v) Subjects who have a Charnley C classification
vi) Subjects who have undergone a contralateral hip replacement within past 6 months
vii) Subjects with a poorly functioning contralateral hip replacement or one which has been identified as requiring revision
viii) The first hip replacement scheduled for subjects identified as requiring primary bi-lateral hip replacements which will not be conducted simultaneously (i.e. on the same day).
i) Subjects who, in the opinion of the Investigator, have an existing condition that would compromise their participation and follow-up in this study.
ii) Women who are pregnant.
iii) Subjects who are known drug or alcohol abusers or with psychological disorders that could effect follow-up care or treatment outcomes.
iv) Subjects who have participated in a clinical study with an investigational product in the last month.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Enduron™ Enduron Standard UHMWPE polyethylene liner in a modular acetabular component Marathon™ Marathon™ Moderately cross-linked polyethylene liner in a modular acetabular component
- Primary Outcome Measures
Name Time Method Evaluate the linear and volumetric wear at the three-year time point. 10yrs post surgery
- Secondary Outcome Measures
Name Time Method Demonstrate the difference in the 3D femoral head displacement between Enduron™ and Marathon™ three-years post-operatively 10yrs post surgery Radiographic analysis 10yrs post surgery Oxford Hip Score 10yrs post surgery SF-12 for Mental and Physical well-being 10yrs post surgery
Trial Locations
- Locations (1)
University Otago, Wellington Medical School of Medicine
🇳🇿Wellington, New Zealand