Clinical Performance of Prime&Bond Active in Self-etch or Selective-etch Mode With or Without Bioglass

NCT ID: NCT03798184

Last Updated: 2019-01-09

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 228 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-11-19
• Study Completion Date: 2021-11-30

Brief Summary

Composite restoration of non-carious cervical lesions has always been a challenge for the clinician, considering that the most frequent cause of failure is retention loss.

Adhesion of composite restoration may be obtained by following four different etching techniques: total-etch in three steps, total-etch in two steps, self-etch in two steps, and self-etch in one step. Nowadays the tendency is to simplify the adhesive classic protocols. With the introduction of universal adhesives such as Prime&Bond Active (Dentsply Sirona) it is possible to obtain a total-etch pattern (enamel and dentine) without the classic etching technique with orthophosphoric acid.

On the other hand, there has been an increase in the awareness of the importance of remaining dental tissue preservation, avoiding preparation of a cavity. This is why it is now preferable to use bioactive glass in order to increase micromechanical retention on the dental surface, instead of the classical approach of preparing the surface with burs.

To date, there are no studies evaluating the clinical performance of the universal adhesive Prime&Bond Active on direct resin composite restoration of non-carious cervical lesions neither in a selective-etch mode (enamel etching) or a self-etch mode (no etching) or using sandblasting with bioactive glass. Therefore, the main objective of the study is to evaluate the retention rate of composite restorations using Prime&Bond Active and a previous sandblasted surface with bioglass in a three-year follow-up, as well as the presence of marginal discoloration, marginal integrity and marginal caries.

Detailed Description

The protocol to be followed in the study is as follows:

1. Obtention of a written informed consent of all participants.

2. Complete medical and dental clinical record.

3. Administration of anesthesia and absolute rubber dam isolation.

4. Cavity cleaning with a prophylactic brush and rubber cup with pumice.

5. Randomly assigning each non-carious cervical lesion to one of the four experimental groups:

5.1. Selective enamel etching and surface roughening with bioglass 5.2. Selective enamel etching without surface roughening. 5.3. Self-etch and surface roughening with bioglass. 5.4. Self-etch without surface roughening.

6. In experimental groups which need surface roughening (group 5.1 and 5.3), sandblasting with bioactive glass will be used in enamel.

7. In experimental groups with selective enamel etch (5.1 and 5.2), 37 % orthophosphoric acid is applied for 15 seconds in enamel, followed by profuse washing with air/water spray for ten seconds and dried using air for 10 seconds without desiccating dentin.

In groups 5.3 and 5.4 this step is omitted.

8. Application of universal adhesive Prime&Bond Active on enamel and dentin for 20 seconds. Subsequently, evaporation of the solvent is realized by applying air for 5 seconds and then light curing for 20 seconds.

9. Application of a "bulk fill" composite resin and light curing, following manufacturer's instructions.

10. Finishing and polishing of the restoration.

11. Monitoring and follow up: visits will be performed at six months, one year, two years and three years. In each evaluation, two independent clinicians who do not participate in the clinical procedures will evaluate each direct composite restoration according to USPHS criteria (Modified United States Public Health Service).

The primary objective is to evaluate the retention of the restoration. The secondary objectives are to evaluate marginal discoloration, marginal integrity and marginal caries.

Conditions

Self-etch; Selective-etch; Bioactive Glass; Direct Resin Composite Restoration; Non-carious Cervical Lesion; Universal Adhesive

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Selective-etch with bioglass surface roughening

Group Type: EXPERIMENTAL

Non-carious cervical lesion restoration

Intervention Type: PROCEDURE

Restoration of non-carious cervical lesions with Prime\&Bond Active in self-etch or selective-etch mode with or without bioglass

Selective-etch without bioglass surface roughening

Group Type: ACTIVE_COMPARATOR

Non-carious cervical lesion restoration

Intervention Type: PROCEDURE

Restoration of non-carious cervical lesions with Prime\&Bond Active in self-etch or selective-etch mode with or without bioglass

Self-etch with bioglass surface roughening

Group Type: EXPERIMENTAL

Non-carious cervical lesion restoration

Intervention Type: PROCEDURE

Restoration of non-carious cervical lesions with Prime\&Bond Active in self-etch or selective-etch mode with or without bioglass

Self-etch without bioglass surface roughening

Group Type: ACTIVE_COMPARATOR

Non-carious cervical lesion restoration

Intervention Type: PROCEDURE

Restoration of non-carious cervical lesions with Prime\&Bond Active in self-etch or selective-etch mode with or without bioglass

Interventions

Non-carious cervical lesion restoration

Restoration of non-carious cervical lesions with Prime\&Bond Active in self-etch or selective-etch mode with or without bioglass

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

1. Patients ≥ 18 years without systemic disease.

2. Presence of a non-carious cervical lesion with a minimum of 1.5 mm in depth and extent to dentin.

3. Non-carious cervical lesions in premolars and molars.

Exclusion Criteria

1. Presence of rampant caries or advanced periodontal disease.

2. Consumption of > 2 cigarette pack/ day.

3. Presence of severe xerostomia or bruxism.

4. Methacrylate allergy.

5. Pregnancy.

Teeth with pulpal and/or periapical pathology, and endodontically treated teeth are excluded from the study.

Teeth with previous pulp capping or previous class V restorations will also be excluded.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Valencia

OTHER

Sponsor Role: lead

Responsible Party

Cristina Pasarín Linares

Teaching Assistant

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

University of Valencia

Valencia, , Spain

Countries

Spain

Other Identifiers

2/2018

Identifier Type: -

Identifier Source: org_study_id