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Effect of occlusal reduction on postoperative pain in teeth with irreversible pulpitis and symptomatic apical periodontitis : A randomized clinical trial / Riham Karam Mohammed Ahmed ; Supervised Nihal Ezzat Sabet , Shaimaa Ismail Gawdat

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Riham Karam Mohammed Ahmed , 2016Description: 93 P. : charts , facsimiles , photographs ; 25cmOther title:
  • تأثير برد السطح الاطباقي للأسنان على إزالة الألم المصاحب لما بعد علاج الجذور فى المرضى ذو التهاب لب السنه غير الردود و التهاب دواعم السنه : تجربة إكلينيكية بالانتقاء العشوائي [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Oral and Dental Medicine - Department of Endodontics Summary: The aim of this study was to assess the effect of occlusal reduction on postoperative pain after endodontic instrumentation and obturation in patients with symptomatic irreversible pulpitis and symptomatic apical periodontitis in mandibular posterior teeth.Materials and methods: 44 patients were included in the study. All patients had posterior mandibular teeth with symptomatic irreversible pulpitis and symptomatic apical periodontitis, pre-operative pain, sensitivity to percussion and with normal periapical radiographic appearance or slight widening in the periodontal membrane space.The patients were randomly assigned into two groups, 22 participants each: The intervention group; where all occlusal contacts on the functional and non-functional cusps as well as on the marginal ridges of the tooth were reduced before starting biomechanical preparation.The control group; where no modification was done for the occlusal surface of the tooth before starting biomechanical preparation. Pain was assessed preoperatively using modified Visual Analogue Scale (VAS). Root canal treatment was accomplished in two visits where root canals were prepared by crown down technique using Revo-S rotary files. Obturation was done using modified single cone technique with resin sealer in the second visit. Pain was assessed at 6, 12, 24 and 48 hours after instrumentation then at 6 and 12 hours after obturation. Patients were given a placebo to be taken in case of moderate or severe pain and ibuprofen 400mg was prescribed in case of persistent pain
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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.09.02.M.Sc.2016.Ri.E (Browse shelf(Opens below)) Not for loan 01010110072697000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.09.02.M.Sc.2016.Ri.E (Browse shelf(Opens below)) 72697.CD Not for loan 01020110072697000

Thesis (M.Sc.) - Cairo University - Faculty of Oral and Dental Medicine - Department of Endodontics

The aim of this study was to assess the effect of occlusal reduction on postoperative pain after endodontic instrumentation and obturation in patients with symptomatic irreversible pulpitis and symptomatic apical periodontitis in mandibular posterior teeth.Materials and methods: 44 patients were included in the study. All patients had posterior mandibular teeth with symptomatic irreversible pulpitis and symptomatic apical periodontitis, pre-operative pain, sensitivity to percussion and with normal periapical radiographic appearance or slight widening in the periodontal membrane space.The patients were randomly assigned into two groups, 22 participants each: The intervention group; where all occlusal contacts on the functional and non-functional cusps as well as on the marginal ridges of the tooth were reduced before starting biomechanical preparation.The control group; where no modification was done for the occlusal surface of the tooth before starting biomechanical preparation. Pain was assessed preoperatively using modified Visual Analogue Scale (VAS). Root canal treatment was accomplished in two visits where root canals were prepared by crown down technique using Revo-S rotary files. Obturation was done using modified single cone technique with resin sealer in the second visit. Pain was assessed at 6, 12, 24 and 48 hours after instrumentation then at 6 and 12 hours after obturation. Patients were given a placebo to be taken in case of moderate or severe pain and ibuprofen 400mg was prescribed in case of persistent pain

Issued also as CD

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