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ACTIVE NOT RECRUITING
NCT04825379
NA

Clinical Evaluation of a Bioactive Material

Sponsor: Hacettepe University

View on ClinicalTrials.gov

Summary

The clinical performance of a bioactive composite and a posterior 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 bioactive composite \[Cention N, Ivoclar Vivadent, Schaan, Liechtenstein (CN)\] and a posterior resin composite \[G-ænial Posterior (GC, Tokyo, Japan) (GP)\] All restorative procedures will be conducted according to manufacturers' instructions. Restorations will be scored using FDI criteria after a week (baseline) 6, 12, 24, 36 and 48 months. Descriptive statistics will be performed using chi-square tests.

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

31

Start Date

2021-06-01

Completion Date

2026-09-01

Last Updated

2025-12-09

Healthy Volunteers

Yes

Conditions

Interventions

DEVICE

bioactive composite

Cention N

DEVICE

posterior composite

G-ænial Posterior

Locations (1)

Hacettepe University

Ankara, Turkey (Türkiye)