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Resin restorations assessment made ??by applying differently the adhesive system

Adhesion of composite resin direct restorations with different protocols of adhesive system application – a clinical study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9p3hdp
Enrollment
Unknown
Registered
2016-03-02
Start date
2015-06-16
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

Caries lesions, needing the replacement of a pre-existing restoration with recurrent Carie lesion, fracture of the restorations. dental caries,dental restoration failure.

Interventions

Each participant (n=50) will receive 3 composite restorations in 3 posterior teeth. Each participant will have a tooth restored in technical 1 (total etching), which is the control group, a tooth rest
Procedure/surgery
E06.323.428

Sponsors

Faculdade de Odontologia da Universidade Federal de Goiás
Lead Sponsor
Faculdade de Odontologia da Universidade Federal de Goiás
Collaborator

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age between 18 and 60 years; both genders; need for Class I and II restorations in premolars and/or molars, presence of at least three dental elements to be restored whose antagonist teeth are present; presence of at least 20 teeth in occlusion.

Exclusion criteria

Exclusion criteria: Holders or removable orthodontic appliances; holders of bruxism; pregnant or breast-feeding.

Design outcomes

Primary

MeasureTime frame
Presence of marginal discoloration in composite restorations clinical assessment (visual inspection), considering a variation of at least 5% in the measurements after the intervention (7 days) and 18 months.

Secondary

MeasureTime frame
Presence of marginal discoloration, fractures and retention, marginal desadaptation, postoperative sensitivity and tooth decay recurrence will be evaluated in the composite restorations clinical assessment (visual inspection), considering a variation of at least 5% in the measurements after the intervention (7 days) and 18 months.

Countries

Brazil

Contacts

Public ContactAndreia Carvalho

Faculdade de Odontologia da Universidade Federal de Goiás

andreia.assiscarvalho@gmail.com556296282625

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Mar 1, 2026