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Evaluation of postoperative pain after irrigation using end-vented navitip tips versus side- vented navitip tips in teeth with irreversible pulpitis : A randomized clinical trial : Part IV / Hoda Nasr Eldin Fawzi Abdullah ; Supervised Suzan Abdulwanees Amin , Marwa Mahmoud Bedier

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Hoda Nasr Eldin Fawzi Abdullah , 2017Description: 112 P. : charts ; 25cmOther title:
  • تقييم ألم ما بعد الإرواء عند استخدام نافيتب نهائى الفتحات مقابل نافيتب جانبى الفتحات مع حالات الإلتهاب اللب الغير ردود : دراسة سريرية عشوائية : الجزء الرابع [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: Objectives: The aim of this prospective randomized clinical trial was to compare the degree of post-operative pain and analgesic intake at 0, 4, 12, 24, 48, 72-h and 7 days after the use of two different irrigation needles. Subjects and Methods: Thirty eight participants diagnosed with symptomatic or asymptomatic irreversible pulpitis in mandibular posterior teeth received single-visit root canal treatment and were divided randomly into two groups according to the type of needle used during irrigation either NaviTip 29-gauge, 27 mm with End-Vented needle (EVN) or NaviTip 31-gauge, 27 mm with Double Sideport Irrigator Tip (SVN). Post-operative pain was measured using Numeric Rating Scale (NRS) pre-operatively, immediate post-operatively and at 4, 12, 24, 48, 72-h and 7 days. Placebo and analgesic intake was recorded at the different time intervals. Results: There was no difference between both groups in the NRS scores at all post-operative time points. A significant increase in pain level was recorded after 4-h compared to the immediate post-operative in the EVN group followed by a gradual decrease in pain levels until pain disappeared at 7 days. No difference in medication (placebo or analgesic) intake post-operatively was recorded between both groups
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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.09.02.M.Sc.2017.Ho.E (Browse shelf(Opens below)) Not for loan 01010110079794000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.09.02.M.Sc.2017.Ho.E (Browse shelf(Opens below)) 79794.CD Not for loan 01020110079794000

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

Objectives: The aim of this prospective randomized clinical trial was to compare the degree of post-operative pain and analgesic intake at 0, 4, 12, 24, 48, 72-h and 7 days after the use of two different irrigation needles. Subjects and Methods: Thirty eight participants diagnosed with symptomatic or asymptomatic irreversible pulpitis in mandibular posterior teeth received single-visit root canal treatment and were divided randomly into two groups according to the type of needle used during irrigation either NaviTip 29-gauge, 27 mm with End-Vented needle (EVN) or NaviTip 31-gauge, 27 mm with Double Sideport Irrigator Tip (SVN). Post-operative pain was measured using Numeric Rating Scale (NRS) pre-operatively, immediate post-operatively and at 4, 12, 24, 48, 72-h and 7 days. Placebo and analgesic intake was recorded at the different time intervals. Results: There was no difference between both groups in the NRS scores at all post-operative time points. A significant increase in pain level was recorded after 4-h compared to the immediate post-operative in the EVN group followed by a gradual decrease in pain levels until pain disappeared at 7 days. No difference in medication (placebo or analgesic) intake post-operatively was recorded between both groups

Issued also as CD

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