Clinical Performance of Thermo-Viscous Bulk-Fill Resin Composite Restorations in Comparison to Conventional Bulk-Fill Resin Composite Restorations in Posterior Teeth A Randomized Control Clinical Trial

Minia University0 sites32 target enrollmentApril 15, 2022

ConditionsCaries,Dental

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Caries,Dental
Sponsor: Minia University
Enrollment: 32
Primary Endpoint: modified United States Public Health Service criteria (USPHS)
Last Updated: 4 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

This clinical trial will be conducted to compare the clinical performance of the thermo-viscous preheated bulk fill composite in the management of carious lesions in posterior teeth in adult patients over 12 months.

Registry

clinicaltrials.gov

Start Date

April 15, 2022

End Date

October 15, 2023

Last Updated

4 years ago

Study Type

Interventional

Study Design

Parallel

Sex

All

Investigators

Sponsor

Minia University

Responsible Party

Principal Investigator

Ahmed Amr Kamal

Assistant lecturer (misr university for sciences and technology)

Minia University

Eligibility Criteria

Inclusion Criteria

•Have at least two molars supported permanent dentition free of any clinically significant occlusal interference and require posterior restoration and fulfilled the inclusion criteria, patients will be informed about the study and will be given an informed consent.
•The two studied materials restorations should be used in approximately the same sized lesions or within the same extensions.
•The patient will be reimbursed for attending for the clinical evaluation(s) of their restorations.
•Be a regular dental attender who agree to return for assessments.

Exclusion Criteria

•There is history of any adverse reaction to clinical materials of the type to be used in the study.
•There was evidence of occlusal parafunction and/or pathological tooth wear.
•Patients whose history revealed parafunctional habits or use of medications that potentially could cause hyposalivation.

Outcomes

Primary Outcomes

modified United States Public Health Service criteria (USPHS)

Time Frame: 1 year

scores A,B,C ( A highest score) (C the lowest score) and overall evaluation for the restorations ( Alpha , bravo, charlie, delta) Alpha for the highest score and delta for the lowest scores