Clinical Investigation Comparing Two Different Ultra-porous Coated Surfaces of Uncemented Cups
Osteoarthritis, Hip
About this trial
This is an interventional treatment trial for Osteoarthritis, Hip focused on measuring Osteoarthritis, Total hip arthroplasty, Uncemented total hip arthroplasty
Eligibility Criteria
Inclusion Criteria: Patients are foreseen for implantation of an uncemented acetabular press-fit cup and an uncemented stem Age 30-70 years Primary osteoarthritis of the hip Body Mass Index between 18 and 35 kg/m2 Willingness and ability to follow clinical investigation protocol Exclusion Criteria: Grossly abnormal hip anatomy (hip dysplasia, Crowe Grade 2 or above, Perthes or other causes) Osteoporosis Paget's disease Inflammatory arthritis Secondary osteoarthritis Presence of malignancy in the area of surgery Treatment with bisphosphonates, cortisol or cytostatic drugs 6 months or less prior to surgery Previous surgery in the affected hip Inclusion of the contralateral hip in this clinical investigation Not suited for the clinical investigation for other reason (surgeon's judgment) Pregnant or breastfeeding women Prison inmate
Sites / Locations
- Volker OttenRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
MobilLINK TrabecuLINK cup
Pinnacle Gription Series 100 cup
The investigational device in this study is the newly developed MobilLINK TrabecuLINK cup. It will in this study be combined with a uncemented LCU stem. The MobilLINK TrabecuLINK cups are made from Tilastan, a Ti6A4V alloy. The MobileLINK press-fit shells are hemispheric and polar flattened. An equatorial press-fit is built into the shells for primary stability after cementless implantation. All shells have a polar hole, which is used to connect an impactor handle for implantation of the shell. This polar hole can be closed with a polar screw. The MobileLINK TrabecuLINK shells have a 3D printed trabecular surface structure with a pore size of 610 to 820 μm and a porosity of 70 %.
For the control group a Pinnacle Gription cup series 100 with a apex hole eliminator will be used together with a neutral cross-linked polyethylene (XLPE) Marathon liner (DePuy Synthes by Johnson & Johnson, Norderstedt, Germany). The Pinnacle Gription cup is a hemispherical, single-geometry, titanium press-fit cup with a solid body. The outer surface consists of a porous coating with 300 μm sintered titanium beads coated with an extra layer of irregularly shaped pure titanium pieces. In cases where no initial stability can be reached when using the Pinnacle 100 series, the Pinnacle Gription sector cup with additional bone screws will be used. The cross-linked Marathon insert is made of 1050 GUR resin, irradiated with 50 kGy, remelted and plasma sterilized. The Pinnacle Gription cup will be implanted together with a Corail stem (DePuy Synthes).