Clinical Trials Logo

Clinical Trial Summary

The goal of this clinical trial is to evaluate the clinical performance of Class II restorations of a thermoviscous nanohybrid materials , of a bulk-fill composite resin, and of conventional nanohyribrid bulk-fill composite resins . Class II restorations will be performed in patients using three different restorative materials.And restorations will be evaluated using modified US Public Health Service criteria Resorations will be photograped and restorations will be evaluated for 6,12 months.


Clinical Trial Description

The aim of this clinical study was to evaluate the clinical performance of Class II restorations of a thermoviscous nanohybrid materials , of a bulk-fill composite resin, and of conventional nanohyribrid bulk-fill composite resins. Methods and Materials: Class II restorations will be performed in patients using three different restorative materials: VisCalor Thermoviscous Bulk-Fill (VCB; a thermoviscous nanohybrid bulk-fill composite resin) , Admira Fusion x-tra ( AFT: a conventional nanohybrid bulk-fill composite resin) and 3M Filtek One Bulk-Fill Restprative (FOB: a conventional bulk-fill nanocomposite ) Futura Bond U adhesive will be used for both conventional bulk-fill composite resin restorations and thermoviscous bulk-fill composite resin restorations. Criteria for inclusion of patients in the study : Healthy individuals without any systemic disease, patients who is between 18 and 60 years old, patiens who brush their teeth 2 times a day,voluntary individuals who have agreed to participate in the study and signed the illuminated consent form, who have been given initial periodontal treatment. Criteria for not inclusion of volunteers in research:Women who are pregnant or breastfeeding ,patienrs with advanced periodontial disease,patiens using a moving segmental prosthesis,patiens who have maloclusions,patiens who have bruxism,patients with known allergies to resin-based restorative materials and binding agents The restorations will be evaluated using modified US Public Health Service criteria in terms of retention, color match, marginal discoloration, anatomic form, marginal adaptation, secondary caries, postoperative sensitivity, and surface texture. Resorations will be photograped and restorations will be evaluated for 6,12 months . ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06212141
Study type Interventional
Source Hacettepe University
Contact
Status Active, not recruiting
Phase N/A
Start date December 12, 2022
Completion date June 15, 2024

See also
  Status Clinical Trial Phase
Not yet recruiting NCT04030117 - Class II Restoration Using Bioactive Restorative Material vs Polyacid Modified Composite Resin in Primary Molars N/A
Completed NCT06393270 - 5-year Clinical Follow-up of Restorative Materials
Not yet recruiting NCT06346795 - Class II Restorations With High-Filled Flowable Composites N/A
Completed NCT05423639 - Influence of Lateral Pressure on Sectional Matrix N/A
Completed NCT06120868 - Comparative Clinical Evaluation Between a Novel Self Adhesive and Conventional Bulk-fill Composites N/A
Not yet recruiting NCT05907928 - Radiographic Evaluation of Adaptation of Universal Adhesives N/A
Active, not recruiting NCT06257108 - Clinical Performance of Bulk-Fill Composite Using With Adhesives With or Without Chlorhexidine N/A
Completed NCT06092567 - Post-operative Sensitivity in Composite Restorations N/A
Completed NCT04943120 - Clinical Evaluation of "Snow-plow"Technique Versus Bulk Fill Technique in Restorations of Class II Cavities N/A