000			03232cam a2200325 a 4500
003			EG-GiCUC
008			210307s2020 ua dh f m 000 0 eng d
040			_aEG-GiCUC _beng _cEG-GiCUC
041	0		_aeng
049			_aDeposite
097			_aM.Sc
099			_aCai01.09.02.M.Sc.2020.Sa.C
100	0		_aSafwa Essam Mohammed Abdelglil
245	1	0	_aComparative evaluation of the effect of prophylactic intraligamentary injection of dexamethasone and piroxicam on postoperative pain in teeth with symptomatic irreversible pulpitis : _bA randomized controlled trial / _cSafwa Essam Mohammed Abdelglil ; Supervised Siza Yacoub Zakhary , Maged M.Negm , Fatma Mohammed Saeed
246	1	5	_aتقييم مقارن لتأثير الحقن الوقائى الذاتى للديكساميثازون و بيروكسيكام على ألم ما بعد العلاج فى الأسنان مع التهاب لب السن غير قابل للعكس : _bتجربة اكلينيكية بالأنتقاء العشوائى
260			_aCairo : _bSafwa Essam Mohammed Abdelglil , _c2020
300			_a124 P. : _bcharts , facsimiles ; _c25cm
502			_aThesis (M.Sc.) - Cairo University - Faculty of Oral and Dental Medicine - Department of Endodontics
520			_aAim: To assess and compare the efficacy of local intraligamentary injection of glucocorticoids (dexamethasone) and NSAID (piroxicam), on postoperative pain in mandibular molars with symptomatic irreversible pulpitis treated in a single visit with a randomized clinical trial. Methods: Forty-two patients were included. After confirming the diagnosis clinically and radiographically, patients were randomly assigned into three equal groups (n=14). After administration of standard inferior alveolar nerve block, each participant received intraligamentary injection of 0.4 ml of either 8 mg/2 ml dexamethasone (experimental group 1), 20 mg/ml piroxicam (experimental group 2) or 20 mg of mepivacaine HCl 36 mg /1.8 ml + Levonordefrin HCl 0.108 mg/ 1.8 ml (comparator). Standard endodontic treatment was performed in a single visit using MPro files with crown-down technique and 2.5% sodium hypochlorite for irrigation and obturated with modified single cone technique using a resin sealer.The pain was assessed using the Numerical Rating scale (NRS) preoperatively, and postoperatively after 4, 6, 12, 24 and 48 hours. All demographic, baseline and outcome data were collected and statistically analyzed. Results: Results showed that there was no statistically significant difference between the three groups regarding age, gender distribution and pre-operative pain. There was a significant reduction in pain in the three groups, however, there was a statistically significant reduction in postoperative pain intensity in the piroxicam group compared to mepivacaine group at all time intervals
530			_aIssued also as CD
653		4	_aDexamethasone
653		4	_aPiroxicam on postoperative pain in teeth
653		4	_aProphylactic
700	0		_aFatma Mohammed Saeed , _eSupervisor
700	0		_aMaged M.Negm , _eSupervisor
700	0		_aSiza Yacoub Zakhary , _eSupervisor
905			_aNazla _eRevisor
905			_aShimaa _eCataloger
942			_2ddc _cTH
999			_c80147 _d80147