Clinical Evaluation of a Restorative Glass Ionomer and a Bulk-fill Composite Resin

N/AActive Not RecruitingNCT04685967

Hacettepe University23 enrolled

Overview

The clinical performance of a restorative glass ionomer and bulk-fill resin composite in class II restorations will be evaluated and compared. After recruiting participants with at least 2 approximal caries lesions, all restorations will be placed by a single clinician. All caries lesions will be removed before restoring. Cavities will be divided into two groups: a restorative glass ionomer \[Equia Forte HT, GC, Tokyo, Japan (EHT)\] and bulk-fill composite resin \[SonicFill2, Orange, CA, USA (SBF)\] All restorative procedures will be conducted according to manufacturers' instructions. Restorations will be scored using modified United States Public Health Service (USPHS) criteria after a week (baseline) 6, 12, 24, 36 and 48 months. Descriptive statistics will be performed using chi-square tests.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

SINGLE

Enrollment

Conditions

Tooth Disease

Interventions

Equia Forte HT, GC, Tokyo, Japan

Bulk-fill compositeDEVICE

SonicFill2, Orange, CA, USA

Eligibility

Sex: ALLMin age: 18 YearsMax age: 65 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * age range will be 18 to 65 * patients should have at least 2 approximal caries lesions require restoration * healthy periodontal status * a good likelihood of recall availability Exclusion Criteria: * poor gingival health * adverse medical history * potential behavioral problems

Locations (1)

Hacettepe University

Ankara, Turkey (Türkiye)

Outcomes

Primary Outcomes

Clinical performances of different restorative systems according to USPHS criteria

Two year results according to USPHS criteria

Time frame: two years

Data from ClinicalTrials.gov

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