Dental abrasion
Conditions
Interventions
This is a blinded two-arm randomized controlled clinical trial. Participants with non-carious cervical lesions in different quadrants will undergo the interventions. The study will have two groups: Gr
washing and drying the cavity
active application of self-etching universal adhesive system
restoration of the cavity with monochromatic composite resin (Vittra Unique and Omnichroma), placed in increments of 1.5mm maximum, followed by light curing for 40s
insertion and light-curing of the composite until filling the cavity. Afterwards, the restorations will be finished immediately with fine and extra-fine diamond burs and polished, under constant cooli
E06.323.428
Sponsors
Universidade Federal dos Vales do Jequitinhonha e Mucuri
Universidade Federal dos Vales do Jequitinhonha e Mucuri
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Adults presenting a non-carious cervical lesion with indication for class V restoration on the buccal surface; Having non-carious cervical lesions in different quadrants; No pain or pulp alteration in the tooth to be restored; Consent to participate in the research
Exclusion criteria
Exclusion criteria: Severe or active periodontal disease; Use fixed orthodontic appliance; rampant caries
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Before and after the restorative procedures, teeth and restorations will have their color evaluated using the VITA Easy shade device (Easyshade®, Vita Zahnfabrik, Bad Säckingen, Germany), following the manufacturer's instructions; or systematically by two examiners, using the VITA 3D Master scale (VITA Zahnfabrik, Bad Säckingen, Germany). Data will be performed immediately, 7, 30, 90 and 180 days after restoration | — |
Secondary
| Measure | Time frame |
|---|---|
| The esthetic properties of the restoration will be evaluated using the modified criteria of the World Dental Federation (FDI) and USPHS. Data will be performed immediately, 7, 30, 90 and 180 days after restoration;Patient satisfaction with the static result will be assessed using a 10cm visual analogue scale. Data will be performed 180 days after restoration | — |
Countries
Brazil
Contacts
Public ContactDhelfeson Oliveira
Universidade Federal dos Vales do Jequitinhonha e Mucuri
Outcome results
None listed