Dental Caries in Children
Conditions
Keywords
Dental caries, Deciduous teeth, Permanent dental restoration
Brief summary
Atypical cavities, which involve more than two surfaces being one of them vestibular or lingual/palatine, are a challenge for restorative dentistry, since the risk of failure of the restorations are related to the number of surfaces involved. Thus, the objective of this project is to conduct a randomized clinical trial in order to evaluate the efficacy and patient-centered outcomes of a chemically-activated alkasite composite resin in atypical lesions of deciduous molars. Deciduous molars of children between 4 and 7 years of age with at least one atypical cavity lesion in deciduous molars will be selected for the ECR. The selected teeth will be randomly divided into two groups: Chemically activated composite resin Alkasite and resin-Modified glass ionomer cement. Clinical and radiographic follow-up of the lesions will be performed for 6 and 12 months. The efficacy of the treatments will be evaluated by the longevity of the restoring procedures and the arrestment of the caries lesions. Patient-centered outcomes will also be evaluated.
Interventions
Selective removal of dental caries with manual instruments, under relative isolation, application of universal adhesive system and restoration with chemically activated composite resin Alkasite.
PROCEDUREDental Restoration with Resin-Modified Glass ionomer Cement
Selective removal of dental caries with manual instruments, under relative isolation, application of polyacrylic acid and restoration with resin-modified glass ionomer cement.
Sponsors
Faculty Sao Leopoldo Mandic Campinas
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Intervention model description
Compare the survival of restorations performed with chemically activated composite resin alkasite and resin- modified glass ionomer cement.
Eligibility
Sex/Gender
ALL
Age
4 Years to 7 Years
Healthy volunteers
Yes
Inclusion criteria
• Children will be included who have at least one posterior tooth with atypical caries lesion.
Exclusion criteria
* Patients with special needs * Patients general health conditions that may affect the oral cavity * Patients non-cooperating in relation to the examination * Patients with orthodontic apparatus * The parents/guardians or children not to consent to their participation in the study. * Teeth with pulp exposure * Teeth with spontaneous pain * Teeth with mobility * Teeth with presence of swelling or fistula close to the tooth * Teeth with furcation or cervical injury * Teeth with restorations, sealants or enamel formation defects will be excluded.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Survival of restoration | 12 months after treatment. | To evaluate the survival of restoration by clinical examination with FDI index. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Secondary caries lesion or on the surface adjacent to the restored tooth | 12 months after treatment. | Presence of caries lesion on the surface adjacent to the restored tooth or on the margins of the restoration by means of visualClinical Examination |
| Perception of children and parents/guardians | 6 months after treatment. | To evaluate the satisfaction of the children in relation to the treatment performed. The questionnaire will be used Child's and parent's questionnaire about teeth appearance. |
| Operator perception | 6 months after the restoration. | It will be employed a questionnaire after the completion of the treatment performed. It will also be added a question about the behavior of children during the procedure, which will be categorized as - great behavior, regular or bad. |
| Caries lesion progression | 12 months after treatment. | For the evaluation of caries progression, the interproximal radiographic examination will be used to verify an increase of radiolucent image under restoration. |
| Child discomfort | Immediately after the treatment. | The child will also be questioned as to the discomfort in relation to the treatment performed. For this will be used the scale of faces of Wong-Baker. |
| Post Operative sensitivity of the child | 7 ° day after the restorative procedure. | The child will also be questioned about the sensitivity of the restorative procedure. For this, the Wong-Baker face scale will be used. |
| Oral health-related quality of life | 6 month of restorative treatment. | The validated Brazilian version of Early Childhood Oral Health Impact Scale (ECOHIS) will be applied to children and should be answered by their parents. |
| Parents/Guardians Satisfaction | 6 months after restoration. | The parents/guardians will be questioned about the satisfaction regarding the treatment performed in the child. The answer will be scored by a likert scale. |
Countries
Brazil
Outcome results
None listed