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
| Type | Name | Description |
|---|---|---|
| DRUG | Selective enamel etching with 36% phosphoric acid | Etch: selective 36% phosphoric acid enamel etching |
| DRUG | No selective enamel etching with 36% phosphoric acid | Non-etch: without phosphoric acid selective enamel etching |
| DEVICE | Clearfil SE Bond | |
| DEVICE | Xeno 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.