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Asperisation of the dental cavity to improve the adhesion of composite resin restorations in patients with proximal teeth lesions of the gingiva

Asperisation of the dental cavity to maximize the adhesion of Composite Resin Restoration in patients with Non-Carious Cervical Lesions (LCNC) - using a Universal Adhesive System in the conventional and self-etching mode: Double Blind Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3cwrdv
Enrollment
Unknown
Registered
2018-02-27
Start date
2018-02-25
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tooth Discoloration. Sensitivity of Dentin. Dental cavity.

Interventions

Conventional Group without asperisation: 47 patients will receive 37% phosphoric acid application for 20 s, suck, wash for 5 seconds, and dry, adhesive application. Conventional Group sprinkled: 47 p
Other

Sponsors

Universidade Estadual do Oeste do Paraná
Lead Sponsor
Universidade Estadual do Oeste do Paraná
Collaborator

Eligibility

Age
No minimum to 0 Years

Inclusion criteria

Inclusion criteria: Patients older than 18 years will be included; presence of at least four LCNCs per patient, regardless of their location in the dental arch; adequate oral hygiene, and absence of driving difficulties that prevent adequate oral hygiene; absence of periodontal disease, active carious lesions and parafunctional habits, at least 20 teeth in function; absence of active staples of removable partial dentures in the teeth included in the research, and that these are not pillars of prostheses; LCNC with a maximum of 50% of enamel margin.

Exclusion criteria

Exclusion criteria: Will be excluded: patients who do not agree with the terms of the survey; patients who do not feel motivated to participate in the research and maintain oral hygiene; patients who have difficulty attending the posterior controls of the restoration

Design outcomes

Primary

MeasureTime frame
Expected outcome 1: Number of restorations that fell after 6 and 12 months.

Secondary

MeasureTime frame
Expected outcome 2: Marginal discoloration will be evaluated on a scale of 1 to 5 proposed by the International Dental Federation (FDI method) after 6 and 12 months.;Expected outcome 3: Marginal adaptation will be assessed on a scale of 1 to 5 proposed by the International Dental Federation (FDI method) after 6 and 12 months.;Expected outcome 4: Caries lesion adjacent to the restoration will be evaluated on a scale of 1 to 5 proposed by the International Dental Federation (FDI method) after 6 and 12 months.;Expected outcome 5: Postoperative sensitivity will be assessed on a scale from 1 to 5 proposed by the International Dental Federation (FDI method) after 6 and 12 months.

Countries

Brazil

Contacts

Public ContactAlessandro Loguercio

Universidade Estadual de Ponta Grossa

aloguercio@hotmail.com55(42)3220-3000

Outcome results

None listed

Source: REBEC (via WHO ICTRP)