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Clinical Trial Summary

The goal of this clinical trial is to evaluate the preheating effect of a group shade resin-based composite. The evaluation will be done on Ryge criteria. The main question it aims to answer is if there is a difference in time between preheated and non-heated resin-based composites in the oral cavity. Participants will be given treatment for cavities class 2 on premolars and molar and will come for recall at 24h, 1 week, 6 weeks, 3 months, 6 months, and 1 year.


Clinical Trial Description

The participants in the study will be adult patients (over 18 years old). Each patient will receive 2 restorations on premolars or molars, class 2, and medium cavities. The restorations will be performed under isolation with rubber-dam, and restored with preheated or not-heated resin-based composite. The occlusion will be tested and they will be notified to come for recall in order to make the evaluation of the restorations. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06251921
Study type Interventional
Source Iuliu Hatieganu University of Medicine and Pharmacy
Contact Corina Prodan, dr.
Phone 0040946981859
Email corinamirelaprodan@gmail.com
Status Recruiting
Phase N/A
Start date January 23, 2024
Completion date March 2025

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