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Comparison between the effect of pulpotec & effect of calcium hydroxide dressings on interappointement pain relief for symptomatic posterior teeth with acute pulpitis and periodontitis / Nassar Hamid Abdullah Alqudaimi ; Supervised Manar Yahia Fouda , Hany Samy Sadek

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Nassar Hamid Abdullah Alqudaimi , 2015Description: 114 P. : charts , facsimiles ; 25cmOther title:
  • وتأثير ضمادات هيدروكسيد الكالسيوم على تخفيف الآلام بين الزيارات للأسنان الخلفية مع أعراض الالتهاب الحاد للعصب والتهاب اللثة PULPOTEC مقارنة بين تأثير [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: Aim: 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 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: Pre-operatively, all cases had severe pain. After 8 hours, Group B showed statistically significantly higher prevalence of no pain and mild pain. Group A showed higher prevalence of mild pain and moderate pain respectively. After 12 hours, Group B showed statistically significantly higher prevalence of no pain. Group A showed higher prevalence of mild pain. After 24 hours, Group B showed statistically significantly higher prevalence of no pain. Group A showed higher prevalence of no pain and mild pain respectively. After 48 hours, all cases had no pain. After 1 month, Group B showed statistically significantly higher prevalence of no pain. Group A 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.Na.C (Browse shelf(Opens below)) Not for loan 01010110075200000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.09.02.M.Sc.2015.Na.C (Browse shelf(Opens below)) 75200.CD Not for loan 01020110075200000

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

Aim: 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 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: Pre-operatively, all cases had severe pain. After 8 hours, Group B showed statistically significantly higher prevalence of no pain and mild pain. Group A showed higher prevalence of mild pain and moderate pain respectively. After 12 hours, Group B showed statistically significantly higher prevalence of no pain. Group A showed higher prevalence of mild pain. After 24 hours, Group B showed statistically significantly higher prevalence of no pain. Group A showed higher prevalence of no pain and mild pain respectively. After 48 hours, all cases had no pain. After 1 month, Group B showed statistically significantly higher prevalence of no pain. Group A showed higher prevalence of severe pain as all cases needed root canal treatment

Issued also as CD

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