NCT04825379

Clinical Evaluation of a Bioactive Material

• Status: Active Not Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 31 (actual)
• Sponsor: Hacettepe University · Academic / Other
• Sex: All
• Age: 18 Years – 65 Years
• Healthy volunteers: Accepted

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.

Conditions

• Tooth Disease

Interventions

Type	Name	Description
DEVICE	bioactive composite	Cention N
DEVICE	posterior composite	G-ænial Posterior

Timeline

• Start date: 2021-06-01
• Primary completion: 2021-09-01
• Completion: 2026-09-01
• First posted: 2021-04-01
• Last updated: 2025-12-09

Locations

1 site across 1 country: Turkey (Türkiye)