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dc.contributor.authorMarkou, N.en
dc.contributor.authorPepelassi, E.en
dc.contributor.authorVavouraki, H.en
dc.contributor.authorStamatakis, H. C.en
dc.contributor.authorNikolopoulos, Georgios K.en
dc.contributor.authorVrotsos, I.en
dc.contributor.authorTsiklakis, K.en
dc.creatorMarkou, N.en
dc.creatorPepelassi, E.en
dc.creatorVavouraki, H.en
dc.creatorStamatakis, H. C.en
dc.creatorNikolopoulos, Georgios K.en
dc.creatorVrotsos, I.en
dc.creatorTsiklakis, K.en
dc.date.accessioned2018-06-22T09:53:57Z
dc.date.available2018-06-22T09:53:57Z
dc.date.issued2009
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/42122
dc.description.abstractBackground: Platelet-rich plasma (PRP) alone or combined with other regenerative materials was previously studied in human periodontal endosseous defects. There are no sufficient data evaluating to what extent the addition of demineralized freeze-dried bone allograft (DFDBA) to PRP may enhance the effectiveness of PRP. The aim of this randomized, double-masked, controlled clinical trial was to compare the effectiveness of autologous PRP alone or a PRP + combination in periodontal endosseous defects. Methods: Twenty-four proximal endosseous defects in 24 patients with severe chronic periodontitis were randomly treated with PRP alone or in combination with DFDBA. The final evaluation at 6 months was based on clinical and radiographic parameters. Subtraction radiography was used. The primary outcome variable was clinical attachment level (CAL). Results: The two treatment groups were initially comparable (mean CAL: 8.67 ± 2.19 mm for PRP + DFDBA and 8.25 ± 1.96 mm for PRP). Both treatments achieved statistically significant and similar CAL gain (3.08 ± 1.17 mm for PRP + DFDBA and 3.08 ± 0.95mmfor PRP), probing depth, defect depth, and area surface reduction. The percentage of defect fill did not significantly differ between the two treatments. There was a non-significant trend to greater defect fill (45.42% versus 41.29%), defect depth (54.05% versus 49.52%), and area surface (58.43% versus 52.16%) reduction with the graft. In both groups, 66.66% of the defects gained ≥3 mm of CAL. Conclusion: Within its limits, this study demonstrated that both PRP and PRP combined with DFDBA resulted in significant clinical and radiographic improvement inhuman periodontal endosseous defects at 6 months, and the addition of DFDBA to PRP did not significantly enhance the treatment outcome. J Periodontol 2009;80:1911-1919.en
dc.language.isoengen
dc.sourceJournal of periodontologyen
dc.subjectMethodologyen
dc.subjectArticleen
dc.subjectHumanen
dc.subjectHumansen
dc.subjectTransplantationen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectControlled studyen
dc.subjectFemaleen
dc.subjectFollow upen
dc.subjectClinical trialen
dc.subjectControlled clinical trialen
dc.subjectTreatment outcomeen
dc.subjectMaleen
dc.subjectFollow-up studiesen
dc.subjectMiddle ageden
dc.subjectComparative studyen
dc.subjectHistologyen
dc.subjectGingiva diseaseen
dc.subjectHomologousen
dc.subjectImage processingen
dc.subjectAllotransplantationen
dc.subjectAlveolar bone lossen
dc.subjectAlveoloplastyen
dc.subjectBone transplantationen
dc.subjectChronic periodontitisen
dc.subjectComputer-assisteden
dc.subjectCryopreservationen
dc.subjectDecalcification techniqueen
dc.subjectDouble blind procedureen
dc.subjectDouble-blind methoden
dc.subjectFreeze dryingen
dc.subjectGingival recessionen
dc.subjectImage processingen
dc.subjectImage subtractionen
dc.subjectOral surgeryen
dc.subjectPeriodontal attachment lossen
dc.subjectPeriodontal diseaseen
dc.subjectPeriodontal pocketen
dc.subjectPlatelet-rich plasmaen
dc.subjectRandomized controlled trialen
dc.subjectRegenerationen
dc.subjectSubtraction techniqueen
dc.subjectThrombocyte rich plasmaen
dc.subjectTissue preservationen
dc.titleTreatment of periodontal endosseous defects with platelet-rich plasma alone or in combination with demineralized freeze-dried bone allograft: A comparative clinical trialen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1902/jop.2009.090216
dc.description.volume80
dc.description.issue12
dc.description.startingpage1911
dc.description.endingpage1919
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidNikolopoulos, Georgios K.[0000-0002-3307-0246]
dc.gnosis.orcid0000-0002-3307-0246


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