A 2-year Clinical Performance of Two Different Ion-releasing Bulk-fill Restorative Materials Posterior Cavities

Mansoura University

Status: Completed

Conditions: Secondary Caries

Treatments: Other: Cention N; Other: Surefil One; Other: Bulkfil resin composite

Study type: Interventional

Funder types: Other

Identifiers

NCT05952609

M02060421

Details and patient eligibility

About

The aim of this study is to evaluate and compare the clinical performance of 2 ion-releasing bulk-fill restorative materials in comparison with a bulk-fill resin composite restoration in posterior cavities.

Enrollment: 32 patients

Sex: All

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Criteria for patient's inclusion in the study will be the presence of at least 3 occlusal or proximal carious lesion in posterior teeth, favourable and stable occlusion between the remaining teeth, the patients must be older than 18 years old with permanent dentition, moderate oral hygiene, asymptomatic vital teeth with no sensitivity to percussion, and the presence of contact with adjacent teeth

Exclusion criteria

• Exclusion criteria will be, sever bruxism, patients with known unavailability to attend recall visits, patients with known allergy to any component of the study materials, pulp exposure during caries excavation, patients with unstable medical conditions and pregnant or lactating individuals.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Double Blind

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32 participants in 3 patient groups

Group 1

Experimental group

Description:

Patients receiving Surefil One

Treatment:

Other: Surefil One

Group 2

Experimental group

Description:

Patients receiving Cention N

Treatment:

Other: Cention N

Group 3

Active Comparator group

Description:

Patients receiving bulkfil resin composite

Treatment:

Other: Bulkfil resin composite