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

Liaquat University of Medical & Health Sciences160 enrolled

Overview

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

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

160

Conditions

Sensitivity, Tooth

Interventions

Tetric N Bond Universal®DRUG

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

Self Etch Tetric N Bond Universal®DRUG

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

GC Fuji IX, GC, Japan®DRUG

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

Eligibility

Sex: ALLMin age: 18 YearsMax age: 40 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: Either gender Minimum age 18 years, maximum age 40 years. Class I \& II Cavity on maxillary and mandibular 1st and 2nd molars. Vital maxillary and mandibular molar teeth that had occlusal contact with antagonist teeth. Exclusion Criteria: Irreversible Pulpitis diagnosed clinically and radiographically. Class I \& Class II cavity of premolars and third molars Patients taking analgesic prior to treatment. History of allergic reaction to any dental material used in the study. History of parafunctional habits (bruxism and/or clenching) Malocclusion

Locations (1)

Institute of Dentistry, Liaquat University of Medical and Health Sciences

Hyderābād, Sindh, Pakistan

Outcomes

Primary Outcomes

Post Operative Sensitivity

Sensitivity will be recorded as present when a patient experienced more pain when the cold stimulus is applied on the restored tooth than on the control tooth is assessed using the modified visual analogue scale to any stimulus (occlusal function, cold/hot water, or sweets) every day by the patient until 7 days, then by the clinician on 7 days, 3 months.

Time frame: 3 Months

Data from ClinicalTrials.gov

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