CERAMENT treatment of fracture defects (CERTiFy) : protocol for a prospective, multicenter, randomized study investigating the use of CERament™ BONE VOID FILLER in tibial plateau fractures

dc.contributor.authorNusselt, Thomas
dc.contributor.authorHofmann, Alexander
dc.contributor.authorWachtlin, Daniel
dc.contributor.authorGorbulev, Stanislav
dc.contributor.authorRommens, Pol Maria
dc.date.accessioned2022-07-11T10:17:27Z
dc.date.available2022-07-11T10:17:27Z
dc.date.issued2014
dc.description.abstractBACKGROUND: Bone graft substitutes are widely used for reconstruction of posttraumatic bone defects. However, their clinical significance in comparison to autologous bone grafting, the gold-standard in reconstruction of larger bone defects, still remains under debate. This prospective, randomized, controlled clinical study investigates the differences in pain, quality of life, and cost of care in the treatment of tibia plateau fractures-associated bone defects using either autologous bone grafting or bioresorbable hydroxyapatite/calcium sulphate cement (CERAMENT™|BONE VOID FILLER (CBVF)). METHODS/DESIGN: CERTiFy (CERament™ Treatment of Fracture defects) is a prospective, multicenter, controlled, randomized trial. We plan to enroll 136 patients with fresh traumatic depression fractures of the proximal tibia (types AO 41-B2 and AO 41-B3) in 13 participating centers in Germany. Patients will be randomized to receive either autologous iliac crest bone graft or CBVF after reduction and osteosynthesis of the fracture to reconstruct the subchondral bone defect and prevent the subsidence of the articular surface. The primary outcome is the SF-12 Physical Component Summary at week 26. The co-primary endpoint is the pain level 26 weeks after surgery measured by a visual analog scale. The SF-12 Mental Component Summary after 26 weeks and costs of care will serve as key secondary endpoints. The study is designed to show non-inferiority of the CBVF treatment to the autologous iliac crest bone graft with respect to the physical component of quality of life. The pain level at 26 weeks after surgery is expected to be lower in the CERAMENT bone void filler treatment group. DISCUSSION: CERTiFy is the first randomized multicenter clinical trial designed to compare quality of life, pain, and cost of care in the use of the CBVF and the autologous iliac crest bone graft in the treatment of tibia plateau fractures. The results are expected to influence future treatment recommendations.en_GB
dc.description.sponsorshipDFG, Open Access-Publizieren Universität Mainz / Universitätsmedizinde
dc.identifier.doihttp://doi.org/10.25358/openscience-7349
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/7363
dc.language.isoengde
dc.rightsCC-BY-2.0*
dc.rights.urihttps://creativecommons.org/licenses/by/2.0/*
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleCERAMENT treatment of fracture defects (CERTiFy) : protocol for a prospective, multicenter, randomized study investigating the use of CERament™ BONE VOID FILLER in tibial plateau fracturesen_GB
dc.typeZeitschriftenaufsatzde
jgu.identifier.pmid24606670
jgu.journal.titleTrialsde
jgu.journal.volume15de
jgu.organisation.departmentFB 04 Medizinde
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternativeArt. 75de
jgu.publisher.doi10.1186/1745-6215-15-75de
jgu.publisher.issn1468-6694de
jgu.publisher.issn1745-6215de
jgu.publisher.issn1468-6708de
jgu.publisher.nameBioMed centralde
jgu.publisher.placeLondonde
jgu.publisher.urihttp://dx.doi.org/10.1186/1745-6215-15-75de
jgu.publisher.year2014
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode610de
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTextde
jgu.type.versionPublished versionde
opus.affiliatedHofmann, Alexander
opus.affiliatedWachtlin, Daniel
opus.affiliatedGorbulev, Stanislav
opus.affiliatedRommens, Pol Maria
opus.date.modified2018-08-08T08:42:27Z
opus.identifier.opusid27338
opus.importsourcepubmed
opus.institute.number0439
opus.institute.number0460
opus.metadataonlyfalse
opus.organisation.stringFB 04: Medizin: Klinik und Poliklinik für Unfallchirurgiede_DE
opus.organisation.stringFB 04: Medizin: Interdisziplinäres Zentrum Klinische Studien Mainz (IZKS)de_DE
opus.subject.dfgcode00-000
opus.type.contenttypeKeinede_DE
opus.type.contenttypeNoneen_EN

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