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العنوان
Clinical Performance of Sonic-Activated ‎Bulk Fill Resin Composite and Dual-Cure ‎Zinc Oxide Containing Bulk Fill Resin ‎Composite as Posterior Restorations /
المؤلف
Ali, Sanya Maised Hussein.
هيئة الاعداد
باحث / سنية مسعد حسين على
مشرف / ياسر فتحى حسين‎ ‎
مشرف / نيرمين السيد محمود‎ ‎
مناقش / شريف عادل محسن‎ ‎
مناقش / إيمان علي سيد أبو عوف
الموضوع
Dentistry. Dentistry, Operative. Dental Caries - therapy. Dental Pulp Diseases - therapy. Dental Restoration, Permanent.
تاريخ النشر
2024.
عدد الصفحات
99 p. :
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
طب الأسنان
تاريخ الإجازة
29/1/2024
مكان الإجازة
جامعة المنيا - كلية طب الأسنان - العلاج التحفظي
الفهرس
Only 14 pages are availabe for public view

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Abstract

The current in vivo study was carried out to assess the clinical performance of two ‎posterior bulk fill resin composite restorative materials for the management of ‎carious class II lesions in adult patients over an up to 6-month evaluation period: ‎sonic activated bulk fill resin composite (Sonicfill2) and a dual cure zinc oxide ‎containing bulk fill resin composite (Fill Up). A convenient sample of twenty ‎patients with proximal caries in at least three of their posterior teeth were chosen. ‎Twenty patients were chosen, and posterior class II cavities were prepared for them. ‎There were two prepared teeth for each patient, for a total of forty prepared teeth. ‎Subsequently, the teeth in each patient were randomly assigned for restoration ‎using resin composite materials without knowledge of the specific allocation as ‎follow: -‎
group A1: Twenty teeth were filled with SonicFill2, a Sonic activated bulk fill ‎resin composite, using the Sonic-fill handpiece, and following the manufacturer’s ‎instructions. The unidose tip was affixed to the cavities and administered into the ‎prepared cavity. ‎
group A2: Following the guidelines provided by the manufacturer, twenty teeth ‎were treated with a Dual cure zinc oxide containing bulk fill resin composite called ‎Fill Up. The material was applied directly into the cavity using an automix syringe ‎and then delivered into the prepared cavity with light pressure. ‎
Evaluation of the restorations
The clinical status of the tested restorations was evaluated at baseline (24h) ‎after placement of the restorations, after one, three and six months.‎
The two types of resin composites were evaluated using Unites State Public ‎Health Service (USPHS) criteria for: -‎
‎1.‎ Color matching (CM).‎
‎2.‎ Marginal discoloration (MD).‎
‎3.‎ Marginal adaptation (MA).‎
‎4.‎ Anatomic form (AF).‎
‎5.‎ Secondary caries (SC).‎
The clinical evaluation conducted by two trained operators and the Alpha and ‎Bravo score percentages were considered significant of clinical success.‎
Evaluation of postoperative sensitivity (POS):‎
Each restored tooth was evaluated for postoperative sensitivity. and the ‎patients’ responses were assessed by using the VAS (Visual Analog Scale) Score. ‎
The results of the study showed that: -‎
‎1-‎ In regard to color match, the results revealed that in SonicFill there was no ‎statistically significant change in color match scores by time. While there was ‎a statistically significant change in color match scores by time in Fill Up.‎
‎2-‎ There were no statistically significant differences between the two tested ‎materials as regards to the marginal discoloration by the time.‎
‎3-‎ There were no statistically significant differences between the two tested ‎materials as regards to the marginal adaptation by the time.‎
‎4-‎ For anatomic form between the two studied materials, no statistically ‎significant differences were found
‎5-‎ No significant differences between the two tested materials for secondary ‎caries.‎
‎6-‎ Regarding postoperative sensitivity, the difference between SonicFill and Fill ‎Up was not statistically significant. At one, three and six months all cases ‎reported no pain in both groups and this result was not significant.‎
‎7-‎ The general results of this clinical study showed that the two tested ‎resin composite materials had a satisfactory significant difference in ‎performance during the evaluation period.‎
Conclusion: ‎
Within the limitations of this current in vivo study, and based on the findings it ‎was concluded that: -‎
‎1-‎ Over the six month follow-up period of the study, both bulk-fill techniques ‎demonstrated satisfactory clinical outcomes throughout the evaluation ‎periods.‎
‎2-‎ The findings of this study indicate that bulk-fill restorations can effectively ‎address the challenges associated with the multi-layer technique. This ‎approach saves time and effort while still achieving satisfactory clinical ‎results.‎
‎3-‎ The two tested bulk-fill resin composite restorative materials exhibited ‎satisfactory clinical performance as a direct restoration for class II cavity ‎preparations.‎
‎ ‎
Recommendations:‎
‎- Because six months may not seem like a long enough period to make an ‎appropriate judgement on restorative material, it is advisable to clinically ‎examine the restorations for extended periods of time in order to provide ‎useful information regarding changes in restorative material over time.‎