Clinical Evaluation of a Self-Adhering Flowable Composite in Class I Cavities

Not Applicable

Completed

• Conditions: Tooth Diseases

• Registration Number: NCT03556553
• Lead Sponsor: Hacettepe University

Brief Summary

The aim of this study is to evaluate long-term clinical performance of a self-adhering flowable resin composite in comparison with a conventional flowable resin composite used with an etch\&rinse adhesive system in minimally invasive class I cavities. Twenty-five patients will receive at least one pair of class I restorations. After class I cavities were prepared they were restored either with a self-adhering flowable resin composite (VertiseFlow/Kerr-VR) or with a flowable resin composite (Luxaflow/DMG-LX) in combination with an etch\&rinse adhesive (Teco/DMG) \[according to the manufacturers' instructions. Restorations will be evaluated at baseline and yearly according to FDI criteria by two evaluaters. Statistical analysis will be carried out with Pearson Chi-Square test and Cochran Q-test followed by Mc Nemar's.

Detailed Description

Not available

Study Timeline

• Study Start: 2011-03-30
• Primary Completion: 2011-06-30
• Study Completion: 2016-06-30
• Study First Submitted: 2018-05-24
• Study First Submitted QC: 2018-06-13
• Study First Posted: 2018-06-14
• Status Verified: 2021-09
• Last Update Submitted: 2021-09-13
• Last Update Posted: 2021-09-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 25

Inclusion Criteria

• having no medical or behavioral problems preventing then from attending review visits, absence of previously placed restorations,having antagonist teeth

Exclusion Criteria

• poor gingival health,uncontrolled, rampant caries,bruxism,removable partial dentures, xerostomia

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Clinical performances of flowable composite resins	Five years	Five year results according to FDIcriteria