Inclusion And Exclusion Criteria For The Eligibility Criteria In Dental

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Eligibility criteria The eligibility criteria can be divided into inclusion and exclusion criteria. Inclusion criteria  Participants should be within the age of 18-55 years at the commencement of the trial.  Have BPE sextant codes less than 3 (i.e. code 0, 1, or 2) in permanent teeth (The British Society of Periodontology, 2011) (refer Appendix 1).  Have at least one permanent tooth with a NCCL.  Have a minimum of 20 natural teeth (these can include crowns and bridges on permanent teeth).  The participant should have good oral hygiene and low caries index (DT<3).  Were generally fit and well, with no systemic conditions or medication that could predispose to periodontal disease. Exclusion Criteria:  Any patients with lesions involving …show more content…

Then, the teeth will be isolated with rubber dam (Hygienic Dental Dam, 2010). High and low volume saliva ejectors will be used additionally for suction of saliva and water from high speed hand piece. During preparation beveling of the enamel margins will be carried out for both groups to increase the surface area of enamel. The same set of burs and instruments will be used for preparation in both groups. Further, for the intervention group the enamel will be selectively etched for 15 seconds with 37% phosphoric acid followed by rinsing and drying of tooth. The one- step adhesive will then be applied to both enamel and dentin (Brady, 2013) with a micro tip applicator. Whereas, for the control group only the 1- step adhesive will be applied onto the prepared cavity. Furthermore, the adhesive will be cured with Mini LED light by Dentsply which has an intensity of 1250 mW/cm² (Adec, 2016). After curing of the bond, composite layering will be carried out by an incremental (0.5mm) placement of composite resin and cured with the same curing light to eliminate bias between the curing efficiency of different lights (Esmaeili, Safarcherati and Vaezi, 2014). Same set of instruments will be used for freehand shaping of composite between groups. A cellulose plastic matrix band and a wedge is used to contour the restoration interproximally (Chandra, S., Chandra, S. and Chandra, G. 2007). A microfilled composite resin [Filtek™ Z250 (3M ESPE)] …show more content…

Marginal integrity has been chosen as the primary outcome measure. Defects and/or gaps at the restoration margins signify poor marginal integrity. The outcome will be measured by modified USPHS (US Public Health Service Guidelines) criteria for direct clinical evaluation [Table 1]. By this the marginal integrity will be scored as Alpha (A), Bravo (B) or Charlie (C) depending on the clinical outcome at baseline followed by every six months for a period of 5 years. The scoring can be done by visual examination along with running an explorer along restoration

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