NCT02631161

Glass Hybrid Versus Composite Restorations of Non-carious Cervical Lesions

Randomized Controlled Trial on Glass Hybrid Versus Composite Restorations of Non-carious Cervical Lesions

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 88 (actual)
• Sponsor: Charite University, Berlin, Germany · Academic / Other
• Sex: All
• Age: 50 Years – 70 Years
• Healthy volunteers: Accepted

Summary

A glass hybrid restorative system (EQUIA forte) clinically compared to a composite resin based material (Clearfil SE Bond, Filtek Supreme XT) for the treatment of dental non-carious cervical lesions.

Detailed description

This is a prospective, randomized, monocenter parallel group study on restoration of tooth with non-carious cervical restorations. Each patient receives cervical restoration(s) either with glass hybrid EQUIA forte or with composite resin/adhesive combination Filtek Supreme XT/Clearfil SE Bond in anterior/posterior tooth region. Restorations will be provided by one experienced operator. One of two independent examiners will evaluate the restorations at baseline (1 week after placement), and after 18, and 36 months according to the FDI criteria. Reliability of examination will be assessed on a random sample of 30 restorations.

Conditions

• Dental Cervical Non-carious Lesion

Interventions

Type	Name	Description
OTHER	Equia Forte	Restoration of cavities with a Glasshybrid material (Equia Forte)
OTHER	Filtek Supreme XT/Clearfil SE Bond	Restoration of cavities with a composite resin based material after placing an adhesive

Timeline

• Start date: 2015-12-01
• Primary completion: 2021-02-01
• Completion: 2021-02-01
• First posted: 2015-12-16
• Last updated: 2021-06-18

Locations

1 site across 1 country: Germany