Vitamin E-enriched medium cross-linked polyethylene in total knee arthroplasty (VIKEP): clinical outcome, oxidation profile, and wear analysis in comparison to standard polyethylene-study protocol for a randomized controlled trial

被引:0
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作者
Maier, Kristin [1 ]
Selig, Marius [1 ]
Haddouche, Andrea [2 ]
Haunschild, Martin [3 ]
Hauschild, Oliver [4 ]
Khalili, Iman [5 ]
Kirschberg, Julia [6 ]
Lutter, Christoph [7 ]
Menges, Michael [8 ]
Mertl, Patrice [9 ]
Niemeier, Andreas [5 ]
Rubens-Duval, Brice [2 ]
Mittelmeier, Wolfram [7 ]
机构
[1] Aesculap AG, Med Sci Affairs, Aesculap Pl, D-78532 Tuttlingen, Germany
[2] CHU Grenoble, Hop Sud, Ave Kimberley, F-38130 Echirolles, France
[3] Kathol Klinikum Koblenz Montabaur, Klin Allgemeine Orthopadie Endoprothet & Kinderor, Kardinal Krementz Str 1-5, D-56073 Koblenz Montabaur, Germany
[4] Pk Klin Weissensee, Dept Orthoped & Trauma Surg, Schonstr 80, D-13086 Berlin, Germany
[5] Krankenhaus Reinbek St Adolf Stift, Hamburger Str 41, D-21465 Reinbek, Germany
[6] Waldkliniken Eisenberg, Klosterlausnitzer Str 81, D-07607 Eisenberg, Germany
[7] Univ Med Rostock, Orthopad Klin & Poliklin, Doberaner Str142, D-18057 Rostock, Germany
[8] Lukas Krankenhaus, Hindenburgstr 56, D-32257 Bunde, Germany
[9] CHU Amiens Picardie, 1 Rond Point Prof Christian Cabrol, F-80054 Amiens 1, France
关键词
Total knee arthroplasty; UHMWPE; Gliding surface material; Clinical study; TOTAL HIP;
D O I
10.1186/s13063-023-07811-1
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundThe gliding surface of total knee endoprostheses is exposed to high loads due to patient weight and activity. These implant components are typically manufactured from ultra-high molecular weight polyethylene (UHMWPE). Crosslinking of UHMWPE by ionizing radiation results in higher wear resistance but induces the formation of free radicals which impair mechanical properties after contact with oxygen. Medium-crosslinked UHMWPE enriched with vitamin E (MXE) provides a balance between the parameters for a sustainable gliding surface, i.e., mechanical strength, wear resistance, particle size, and oxidation stability. Therefore, a gliding surface for knee endoprostheses made up from this material was developed, certified, and launched. The aim of this study is to compare this new gliding surface to the established predecessor in a non-inferiority design.MethodsThis multicenter, binational randomized controlled trial will enroll patients with knee osteoarthritis eligible for knee arthroplasty with the index device. Patients will be treated with a knee endoprosthesis with either MXE or a standard gliding surface. Patients will be blinded regarding their treatment. After implantation of the devices, patients will be followed up for 10 years. Besides clinical and patient-related outcomes, radiological data will be collected. In case of revision, the gliding surface will be analyzed biomechanically and regarding the oxidative profile.DiscussionThe comparison between MXE and the standard gliding surface in this study will provide clinical data to confirm preceding biomechanical results in vivo. It is assumed that material-related differences will be identified, i.e., that the new material will be less sensitive to wear and creep. This may become obvious in biomechanical analyses of retrieved implants from revised patients and in radiologic analyses.Trial registrationClinicalTrials.gov, NCT04618016. Registered 27 October 2020, https://clinicaltrials.gov/study/NCT04618016?term=vikep&checkSpell=false&rank=1.All items from the World Health Organization Trial Registration Data Set can be found in Additional file 1.Trial registrationClinicalTrials.gov, NCT04618016. Registered 27 October 2020, https://clinicaltrials.gov/study/NCT04618016?term=vikep&checkSpell=false&rank=1.All items from the World Health Organization Trial Registration Data Set can be found in Additional file 1.
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