Clinical Performance of Thermoviscous Bulk Fill Resin Composites in Comparison to Conventional Packable Bulk Fills
- 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
-
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.
- 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
Group Intervention Description thermoviscous bulk fill resin composite thermoviscous bulkfill composite (Viscalor) - conventional bulk fill resin composite thermoviscous bulkfill composite (Viscalor) -
- Primary Outcome Measures
Name Time Method 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
Name Time Method post operative senstivity 1 week