Tomographic assessment of bone changes in atrophic maxilla treated by split-crest technique and dental implants with plateletrich fibrin and NanoBone® versus platelet-rich fibrin alone: Randomized controlled trial

dc.AffiliationOctober University for modern sciences and Arts MSA
dc.contributor.authorAnis, Maged 
dc.contributor.authorAbdelrahman, Ahmed Reda 
dc.contributor.authorAttia, Rasha 
dc.contributor.authorZahran, Amr 
dc.date.accessioned2024-06-22T10:57:24Z
dc.date.available2024-06-22T10:57:24Z
dc.date.issued2024-06
dc.description.abstractBackground: This study evaluated the clinical benefits of adding NanoBone® with split-crest technique and simultaneous implant placement covered with platelet-rich fibrin membrane in horizontally deficient maxillary ridges in terms of crestal and horizontal bone changes and patient morbidity. Methods: Forty patients indicated for maxillary ridge splitting and simultaneous implant placement were assigned randomly to the study groups: control group (Platelet Rich Fibrin membrane) and test group (Platelet Rich Fibrin membrane + Nanobone®). The Cone Beam Computed Tomography Fusion technique was utilized to assess crestal and horizontal bone changes after five months of the surgical procedure. Patient morbidity was recorded for one week post-surgical. Results: Five months post-surgical, buccal crestal bone resorption was 1.26 ± 0.58 mm for the control group and 1.14 ± 0.63 mm for the test group. Lingual crestal bone resorption was 1.40 ± 0.66 mm for the control group and 1.47 ± 0.68 mm for the test group. Horizontal bone width gain was 1.46 ± 0.44 mm for the control group and 1.29 ± 0.73 mm for the test group. There was no significant statistical difference between study groups regarding crestal and horizontal bone changes and patient morbidity. Conclusions: The tomographic assessment of NanoBone® addition in this study resulted in no statistically significant difference between study groups regarding crestal and horizontal bone changes and patient morbidity. More randomized controlled clinical trials on gap fill comparing different bone grafting materials versus no grafting should be conducted. Clinicaltrials.gov registration number: NCT02836678, 13th January 2017.en_US
dc.description.urihttps://www.scimagojr.com/journalsearch.php?q=24341&tip=sid&clean=0
dc.identifier.doihttps://doi.org/10.1186/s12903-024-04420-5
dc.identifier.otherhttps://doi.org/10.1186/s12903-024-04420-5
dc.identifier.urihttp://repository.msa.edu.eg/xmlui/handle/123456789/6065
dc.language.isoenen_US
dc.publisherBioMed Central Ltden_US
dc.relation.ispartofseriesBMC Oral Health;Volume 24, Issue 1December 2024 Article number 691
dc.subjectAlveolar ridge augmentation; Crestal bone changes; Dental implant; Nanocrystalline hydroxyapatite; Piezo-electric surgery; PRF; Ridge splittingen_US
dc.titleTomographic assessment of bone changes in atrophic maxilla treated by split-crest technique and dental implants with plateletrich fibrin and NanoBone® versus platelet-rich fibrin alone: Randomized controlled trialen_US
dc.typeArticleen_US

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