Dentin Treatments for Restorations of Cervical Lesions Non-Carious
Adhesion
About this trial
This is an interventional treatment trial for Adhesion focused on measuring Non-carious cervical lesions, Randomized clinical trial, Permanent dental restoration, Dentin, Adhesion, Restoration, Sensitivity, Prophylaxis, Randomized
Eligibility Criteria
Inclusion Criteria:
- Presence of at least three non-carious cervical lesions on the buccal aspect of previous vital teeth or premolars;
- Visible plaque index presence and / or gingival bleeding index of at most 20%;
- Probing depth of at least 3 mm in the experimental site and / or buccal 4 mm in any place;
- Patients with good general health condition;
- Patients able to understand and sign the letter of information and the free and informed consent;
- Patients willing to return every six months to revaluation queries.
Exclusion Criteria:
- Presence of less than 20 teeth in the mouth;
- Patients undergoing orthodontic treatment;
- Patients with occlusion problems;
- Veneers with wear over 50% of the incisal / occlusal structure;
- Absence of tooth antagonist.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Other
Experimental
Experimental
Treatment of Dentin Surface
Dentin Surface
Treatment
Treatment of Dentin Surface: Restoration made following the protocol recommended by the manufacturer of the materials.
Treatment of Dentin Surface: Increased etching dentin for 15 seconds to 30 seconds
Treatment of Dentin Surface: Intervention with the cavity prophylaxis probe ultrasound blunt applied for 30 seconds in Surface hypermineralized non-carious dentin cervical lesions. Therefore, the restoration was done following the protocol recommended by the manufacturer of the material.