header
Image from OpenLibrary

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 V / Nashwa Hassan Amin Hosny ; Supervised Suzan Abdulwanees Amin , Marwa Mahmoud Bedier

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Nashwa Hassan Amin Hosny , 2018Description: 106 P. : charts , facsimiles ; 25cmOther title:
  • تقييم ألم مابعد الإرواء عند استخدام نافيتب نهائى الفتحات مقابل نافيتب جانبى الفتحات مع حالات الإلتهاب اللب الغير ردود : دراسة سريرية عشوائية الجزء الخامس [Added title page title]
Subject(s): Available additional physical forms:
  • Issued also as CD
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 Side-port 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 a statistically significance difference in post-operative pain between both groups at 12, 24, 48 and 72-h post-operatively. A significant increase in pain level was recorded after4-h compared to the immediate post-operative in the end-vented needle group, followed by a gradual decrease in pain levels until pain disappeared at 7 days with no difference in medication (placebo and/or analgesic) intake post-operatively between both groups
Tags from this library: No tags from this library for this title. Log in to add tags.
Star ratings
    Average rating: 0.0 (0 votes)
Holdings
Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.09.02.M.Sc.2018.Na.E (Browse shelf(Opens below)) Not for loan 01010110077296000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.09.02.M.Sc.2018.Na.E (Browse shelf(Opens below)) 77296.CD Not for loan 01020110077296000

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 Side-port 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 a statistically significance difference in post-operative pain between both groups at 12, 24, 48 and 72-h post-operatively. A significant increase in pain level was recorded after4-h compared to the immediate post-operative in the end-vented needle group, followed by a gradual decrease in pain levels until pain disappeared at 7 days with no difference in medication (placebo and/or analgesic) intake post-operatively between both groups

Issued also as CD

There are no comments on this title.

to post a comment.