Clinical Trials Directory

Trials / Completed

CompletedNCT02419157

Selective Enamel Etching in Self-etching Adhesives: a 2-year Clinical Trial

Effectiveness of One- and Two-step Self-etching Adhesives Applied With or Without Selective Enamel Etching: a 2-year Randomized Controlled Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
25 (actual)
Sponsor
University of Guarulhos · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the clinical effectiveness of non-carious cervical lesions (NCCLs) restored with two self-etching adhesive systems applied with or without selective enamel etching.

Detailed description

The purpose of this study is to evaluate the clinical effectiveness of non-carious cervical lesions (NCCLs) restored with two self-etching adhesive systems: Clearfil SE Bond (Kuraray Noritake, Japan) and Xeno V + (Dentsply De Trey, Germany) applied with or without 36% phosphoric acid enamel etching. Assessments were at baseline, 3, 6, 12, 18 and 24 months of clinical service.

Conditions

Interventions

TypeNameDescription
DRUGSelective enamel etching with 36% phosphoric acidEtch: selective 36% phosphoric acid enamel etching
DRUGNo selective enamel etching with 36% phosphoric acidNon-etch: without phosphoric acid selective enamel etching
DEVICEClearfil SE Bond
DEVICEXeno V

Timeline

Start date
2012-10-01
Primary completion
2014-10-01
Completion
2014-10-01
First posted
2015-04-17
Last updated
2015-04-17

Source: ClinicalTrials.gov record NCT02419157. Inclusion in this directory is not an endorsement.