Dental Restoration Failure, Dental Restorations Longevity, Esthetics, Dental
Conditions
Brief summary
The objective of this double-blind randomized clinical trial is to evaluate the influence of caries risk, occlusal stress and missing teeth on anterior restorations over a 10 years follow up period. 300 teeth will be randomized according to two adhesive systems: Single Bond 2 and Single Bond Universal (3M ESPE); and two composite resins: nanoparticulated (Filtek ™ Z-350- 3M ESPE) and nanohybrid (IPS Empress Direct - Ivoclar Vivadent). The randomization will be stratified according to the risk of caries and cavity type. The primary outcomes will be longevity, annual failure rate (AFR) and the success of the restorations, and the secondary outcome will be causes for restorations' failure.
Interventions
PROCEDURERestorations with nanoparticulated composites and self etch adhesives
The restorations will be placed according to the protocol developed for the care, following the guidelines of the manufacturers, with a self-etching dental adhesive (SingleBond Universal, 3M ESPE), selective enamel etching, and use of a nanoparticulated composite (Z350, 3M ESPE)
PROCEDURERestorations with nanoparticulated composites and total-etch adhesives
The restorations will be placed according to the protocol developed for the care, following the guidelines of the manufacturers, with a total-etching dental adhesive (SingleBond 2, 3M ESPE), and use of a nanoparticulated composite (Z350, 3M ESPE)
PROCEDURERestorations with nanohybrid composites and self etch adhesives
The restorations will be placed according to the protocol developed for the care, following the guidelines of the manufacturers, with a self-etching dental adhesive (SingleBond Universal, 3M ESPE), selective enamel etching, and use of a nanohybrid composite (IPS Empress Direct, Ivoclar Vivadent).
PROCEDURERestorations with nanohybrid composites and total-etch adhesives
The restorations will be placed according to the protocol developed for the care, following the guidelines of the manufacturers, with a total-etching dental adhesive (SingleBond 2, 3M ESPE), and use of a nanohybrid composite (IPS Empress Direct, Ivoclar Vivadent).
Sponsors
Federal University of Pelotas
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)
Intervention model description
This study is a prospective randomized clinical trial, triple-blind, (patients, investigator and clinical evaluator) with parallel groups. After completing the ICDAS (International Caries Detection and Assessment), clinical occlusal stress examination and questionnaire application on occlusal stress, patients will be randomly divided into two types of dental adhesives and two types of composite resin. Randomization will be stratified according to the risk of caries determined by the ICDAS and the type of cavity to be filled. Operators (Master students and undergraduate students from the last year of the School of Dentistry, Federal University of Pelotas) will place the restorations supervised by highly trained clinicians.
Eligibility
Sex/Gender
ALL
Age
9 Years to 70 Years
Healthy volunteers
Yes
Inclusion criteria
* Patients with restorative needs in anterior teeth; * Patients able to understand and sign the informed consent form; * Patients willing to return to follow up.
Exclusion criteria
* Patients who had a need for Class III and Class IV restorations that did not involve at least 1/3 of the tooth; * Patients under orthodontic treatment; * Patients with a compromised general health condition, presenting a greater risk than ASA II, according to the ASA-PS (American Society of Anesthesiologists - Physical Status); * Patients who had no occlusal contact with an opposing tooth and/or crown; * Patient with absence of bilateral balanced occlusion; * Patient with deep caries lesions in close contact with the dental pulp and in need of expectant treatment or direct pulp capping; * Patients with post-retained need in anterior teeth.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Survival of the restorations | Changes in the dental restorations status compared to baseline will be assessed yearly up to 10 years. | Survival of the restoration is defined as any case where the restoration remains functional in the mouth at the time of evaluation, regardless of need of small interventions, such as repair or refurbishment. The restorations were evaluated shortly after baseline and in prospective periods through a direct clinical inspection, with an explorer probe and a clinical mirror, according to the criteria for clinical evaluation of restorations proposed by the FDI (International Dental Federation) (Hickel et al., 2010), the risks of caries and occlusal stress were also evaluated again. Two trained and calibrated evaluators, unrelated to making the restorations, blinded to the type of material used, independently performed the clinical evaluations. |
| Success of the restorations | Changes in the dental restorations status compared to baseline will be assessed yearly up to 10 years. | Success of the restoration is defined as any case where the restoration remains functional in the mouth at the time of evaluation, without any need of new interventions, and attending the patients demands. The restorations were evaluated shortly after baseline and in prospective periods through a direct clinical inspection, with an explorer probe and a clinical mirror, according to the criteria for clinical evaluation of restorations proposed by the FDI (International Dental Federation) (Hickel et al., 2010), the risks of caries and occlusal stress were also evaluated again. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Patient satisfaction with the treatment | Changes in the patient's satisfaction status compared to baseline will be assessed yearly up to 10 years. | Patient satisfaction will be recorded with FDI criteria |
Countries
Brazil
Outcome results
None listed