drugset / Trial / NCT05882760

Postoperative Sensitivity Following Placement with Different Restorative Materials in Vital Posterior Teeth

NCT05882760 ↗

Phase 4 Completed 160 enrolled Liaquat University of Medical & Health Sciences
NaParallel-groupDouble-blindTreatment

Summary

There is a lack of long-term clinical studies comparing different restorative materials; most of the available studies have only looked at class I cavities or examined post-operative sensitivity in non-caries cervical lesions. The purpose of this study is to measure postoperative sensitivity in clinical settings at 3-month intervals for class 1 and 2 direct posterior restoration

Timeline

Start
2023-06-01
Primary completion
2024-09-30
Completion
2024-12-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Activa TM Bioactive Restorative ® Unknown — —
Comparator GC Fuji IX Unknown — —
Comparator Tetric N Bond Universal® Unknown — —

Indications