Clinical Trials Directory

Trials / Unknown

UnknownNCT02991664

Clinical Performance of a Glass-ionomer Restorative System in Extended-sized Cavities

Randomized, Controlled Trial of Glass Ionomer System vs Composite Posterior Restorations in Extended Sized Class 2 Cavities

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Hacettepe University · Academic / Other
Sex
All
Age
20 Years – 50 Years
Healthy volunteers
Accepted

Summary

The aim of this clinical trial was to compare the clinical performances of a glass ionomer restorative system with a micro hybrid resin based composite in extended sized class II cavities. A total of 100 class 2 lesions were restored with a glass ionomer restorative system (Equia Forte) or a micro hybrid composite (G-aenial Posterior). Restorations were evaluated at baseline and yearly during 6 years according to the modified-USPHS criteria. Data were analyzed with Cohcran's Q and McNemar's tests (p\<0.05).

Detailed description

Since the introduction of glass ionomers many modifications of these materials have been performed over the years. Compared to other permanent filling materials like resin-based composites, glass ionomers show several advantages, such as the ability to adhere to moist enamel and dentin and anti-cariogenic properties such as the long-term fluoride release. So, it was doubtful that glass ionomers represent a capable counterpart of amalgam or resin-based composites in posterior teeth.

Conditions

Interventions

TypeNameDescription
OTHEREquia ForteGlass ionomer restorative system
OTHERG-aenial PosteriorMicro hybrid composite resin

Timeline

Start date
2015-12-01
Primary completion
2016-12-01
Completion
2021-12-01
First posted
2016-12-13
Last updated
2016-12-13

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT02991664. Inclusion in this directory is not an endorsement.