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Active Not RecruitingNCT04685967

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

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

Summary

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.

Conditions

Interventions

TypeNameDescription
DEVICEGlass ionomerEquia Forte HT, GC, Tokyo, Japan
DEVICEBulk-fill compositeSonicFill2, Orange, CA, USA

Timeline

Start date
2021-03-15
Primary completion
2021-08-15
Completion
2026-08-15
First posted
2020-12-28
Last updated
2025-12-03

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT04685967. Inclusion in this directory is not an endorsement.