Assessment of postoperative pain after using reciproc versus one shape niti systems in patients with symptomatic irreversible pulpitis : A randomized clinical trial - part 1 / Michel Karam Eissa Elias ; Supervised Hebatallah Mohamed Maged Elfar , Shaimaa Ismail Gawdat
Material type: TextLanguage: English Publication details: Cairo : Michel Karam Eissa Elias , 2018Description: 100 P. : charts , facsimiles ; 25cmOther title:- تقييم الألم بعد العمل على انظمة التوسيع الآلي باستخدام نظام ريسبروك و نظام وان شيب المصنوع من النيكل تيتانيوم مع مرضى التهاب اللبّ غير الردود العرضي : تجربة إكلينيكية بالانتقاء العشوائي - الجزء الأول [Added title page title]
- Issued also as CD
Item type | Current library | Home library | Call number | Copy number | Status | Date due | Barcode | |
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Thesis | قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.09.02.M.Sc.2018.Mi.A (Browse shelf(Opens below)) | Not for loan | 01010110077981000 | |||
CD - Rom | مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.09.02.M.Sc.2018.Mi.A (Browse shelf(Opens below)) | 77981.CD | Not for loan | 01020110077981000 |
Thesis (M.Sc.) - Cairo University - Faculty of Oral and Dental Medicine - Department of Endodontics
Introduction: The purpose of this study was to assess the postoperative pain and the intake of analgesic medication after using Reciproc single-file reciprocating system or One Shape continuous rotary system in patients with symptomatic irreversible pulpitis with a randomized clinical trial. Subjects and methods: 54 patients with symptomatic irreversible pulpitis in mandibular premolar teeth were included. After confirming the diagnosis clinically and radiographically, patients were randomly assigned into two equal groups of 27 patients each. In the intervention group, root canals were prepared with Reciproc reciprocating single-file (40/.06), whereas the comparator group was prepared with One Shape rotary system (25/.06 and then finished with 30/.06 and 37/.06). Endodontic treatment was performed in single visit with 2.5% sodium hypochlorite for cleaning and lateral condensation technique with resin sealer for obturation. Pain was assessed pre-operatively, then postoperatively immediately at the end of treatment and after 6, 12, 24, 48 and 72 hours. Numerical Rating Scale (NRS) was used as the primary outcome measure. Patients were given an analgesic (Ibuprofen 200 mg) in case of severe pain. All demographic data and NRS scores were collected from the patients and statistically analyzed
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