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Comparison between the effect of pulpotec and effect of calcium hydroxide dressings on interapointement pain relief for symptomatic posterior teethwith acute pulpitis and periodontitis / Nesrin Mohamed Raafat Abuelnasr ; Supervised Manar Yehia Fouda , Hany Samysadek

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Nesrin Mohamed Raafat Abuelnasr , 2015Description: 133 P. : charts , facsimiles ; 25cmOther title:
  • وبين ضمادات هيدروكسيد الكالسيوم على تخفيف الآلام بين الزيادات للاسنان الخلفية مع الالتهاب الحاد للعصب والتهاب اللثة الجزء السابعPulpotecالمقارنة بين تاثير [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 compare the effect of pulpotec and calcium hydroxide intracoronal dressing on inter-appointment pain relief for symptomatic posterior teeth with acute pulpitis with apical periodontitis. Materials and methods: The trial design followed the CONSORT 2010 flow diagram; the participants in this research were assigned into two groups, 22 patients in each group: randomly divided into two equal groups: GROUP A: will receive Calcium Hydroxide dressing GROUP B: will receive Pulpotec dressing. All selected participant subjected to Pulpotomy mechanically by removal of the irritant from the pulp chamber with leaving intact vital radicular pulp then chemically by using one of the comparable medicaments according to the allocated group followed by zinc phosphate base and restored finally with amalgam for all the teeth. The primary outcome that was the degree of pain relieving after the procedure by 8, 12, 24, 48 hours was measured using the Visual Analogue Scale (VAS). Secondary outcome that was follow up visits to determine the intervention results by time on pain using the (VAS) and to evaluate its effect clinically and radiographically after 1month, 3months and 6months. Results: The study resulted in after 8 hours,Group B showed higher prevalence of no pain, mild pain as well as severe pain. Group A showed higher prevalence of moderate pain.After12 hours,Group B showed higher prevalence of no pain and severe pain. Group A showed higher prevalence of mild pain. After 24 hours, Group B showed higher prevalence of no pain than Group A, which showed higher prevalence of mild pain. After 48 hours, all cases had no pain. After 1 month, Group B showed higher prevalence of no pain in comparison with Group A, which showed higher prevalence of severe pain as all cases needed root canal treatment.
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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.09.02.M.Sc.2015.Ne.C (Browse shelf(Opens below)) Not for loan 01010110068686000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.09.02.M.Sc.2015.Ne.C (Browse shelf(Opens below)) 68686.CD Not for loan 01020110068686000
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Cai01.09.02.M.Sc.2015.Ne.B Bond degradation resistance and interface characterization of a water-expandable endodontic obturation point / Cai01.09.02.M.Sc.2015.Ne.B Bond degradation resistance and interface characterization of a water-expandable endodontic obturation point / Cai01.09.02.M.Sc.2015.Ne.C Comparison between the effect of pulpotec and effect of calcium hydroxide dressings on interapointement pain relief for symptomatic posterior teethwith acute pulpitis and periodontitis / Cai01.09.02.M.Sc.2015.Ne.C Comparison between the effect of pulpotec and effect of calcium hydroxide dressings on interapointement pain relief for symptomatic posterior teethwith acute pulpitis and periodontitis / Cai01.09.02.M.Sc.2015.Ne.E Effect of 4% articaine infiltration versus 2% lidocaine nerve block after premedication by lbuprofen on anesthetic effic endodontic treatment of acute Irreversible pulpiti : A randomized clinical trial part III / Cai01.09.02.M.Sc.2015.Ne.E Effect of 4% articaine infiltration versus 2% lidocaine nerve block after premedication by lbuprofen on anesthetic effic endodontic treatment of acute Irreversible pulpiti : A randomized clinical trial part III / Cai01.09.02.M.Sc.2015.Ra.E Evaluation of antimicrobial efficacy of four medicinal plants extract used as root canal irrigant on enterococcus faecalis : An in vitro study /

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

The aim of this study was to compare the effect of pulpotec and calcium hydroxide intracoronal dressing on inter-appointment pain relief for symptomatic posterior teeth with acute pulpitis with apical periodontitis. Materials and methods: The trial design followed the CONSORT 2010 flow diagram; the participants in this research were assigned into two groups, 22 patients in each group: randomly divided into two equal groups: GROUP A: will receive Calcium Hydroxide dressing GROUP B: will receive Pulpotec dressing. All selected participant subjected to Pulpotomy mechanically by removal of the irritant from the pulp chamber with leaving intact vital radicular pulp then chemically by using one of the comparable medicaments according to the allocated group followed by zinc phosphate base and restored finally with amalgam for all the teeth. The primary outcome that was the degree of pain relieving after the procedure by 8, 12, 24, 48 hours was measured using the Visual Analogue Scale (VAS). Secondary outcome that was follow up visits to determine the intervention results by time on pain using the (VAS) and to evaluate its effect clinically and radiographically after 1month, 3months and 6months. Results: The study resulted in after 8 hours,Group B showed higher prevalence of no pain, mild pain as well as severe pain. Group A showed higher prevalence of moderate pain.After12 hours,Group B showed higher prevalence of no pain and severe pain. Group A showed higher prevalence of mild pain. After 24 hours, Group B showed higher prevalence of no pain than Group A, which showed higher prevalence of mild pain. After 48 hours, all cases had no pain. After 1 month, Group B showed higher prevalence of no pain in comparison with Group A, which showed higher prevalence of severe pain as all cases needed root canal treatment.

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