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

NCT02419157 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2015-04-17

No results posted yet for this study

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.

Conditions

  • Selective Enamel Etching in Dental Restorations

Interventions

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

Sponsors & Collaborators

  • University of Guarulhos

    lead OTHER

Principal Investigators

  • André F Reis · University of Guarulhos

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-10-31
Primary Completion
2014-10-31
Completion
2014-10-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02419157 on ClinicalTrials.gov