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

NCT05882760 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 160

Last updated 2025-03-06

No results posted yet for this study

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

Conditions

  • Sensitivity, Tooth

Interventions

DRUG

Tetric N Bond Universal®

Cavities will be restored with Conventional Hybrid Composite Restoration bonded with Etch \& Rinse Tetric - N - Bond (Ivoclar)

DRUG

Self Etch Tetric N Bond Universal®

Cavities will be restored with Conventional Hybrid Composite Restoration bonded with Self Etch Tetric N Bond Universal®

DRUG

GC Fuji IX, GC, Japan®

Cavities will be restored with GC Fuji IX, GC, Japan®

DRUG

Activa TM Bioactive Restorative ®

Cavities will be restored with Activa TM Bioactive Restorative ®

Sponsors & Collaborators

  • Liaquat University of Medical & Health Sciences

    lead OTHER

Principal Investigators

  • Priya Rani, BDS · Liaquat University of Medical and Health Science

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

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

Countries

  • Pakistan

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05882760 on ClinicalTrials.gov