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Clinical Performance of Thermoviscous Bulk Fill Resin Composites in Comparison to Conventional Packable Bulk Fills

Not Applicable
Conditions
Caries,Dental
Interventions
Other: thermoviscous bulkfill composite (Viscalor)
Registration Number
NCT05276154
Lead Sponsor
Minia University
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
32
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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
thermoviscous bulk fill resin compositethermoviscous bulkfill composite (Viscalor)-
conventional bulk fill resin compositethermoviscous bulkfill composite (Viscalor)-
Primary Outcome Measures
NameTimeMethod
modified United States Public Health Service criteria (USPHS)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

Secondary Outcome Measures
NameTimeMethod
post operative senstivity1 week
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