Composite Resins
Conditions
Interventions
This is a randomized, double-blind (patient and evaluator), parallel, equivalence clinical trial. It will be conducted in the clinics of the Dentistry Program at the State University of Ponta Grossa.
Sponsors
Universidade Estadual de Ponta Grossa
Universidade Estadual de Ponta Grossa
Eligibility
Age
3 Years to 10 Years
Inclusion criteria
Inclusion criteria: Good general and oral health; no need for endodontic or periodontal treatment; patients between three and ten years old who require a restoration in a primary posterior tooth; any gender
Exclusion criteria
Exclusion criteria: Severe systemic diseases; poor oral hygiene; allergy to any components present in the materials used; patients with a high risk of pulp exposure; endodontic complications; chronic use of medications
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of this clinical study is the fracture/retention of the restorations over time. This will be assessed by experienced and calibrated evaluators following FDI criteria. The fracture/retention of the restorations will be compared between the control group and the test group through visual inspection of each restoration | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcomes will also be evaluated following FDI criteria, including marginal adaptation, post-operative sensitivity, recurrence of carious lesions, color, surface polish, occlusion and wear, proximal contact (in the case of Class II), anatomical form, and radiographic evaluation, as well as patient satisfaction with the restorative procedure in both groups. These outcomes will also be assessed by experienced and calibrated blinded evaluators through visual and radiographic means | — |
Countries
Brazil
Contacts
Public ContactAna Chibinski
Universidade Estadual de Ponta Grossa
Outcome results
None listed