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Clinical performance of a composite resin with intelligent chromatic technology for the restoration

Clinical performance of a composite resin with intelligent chromatic technology for the restoration of non-carious cervical lesions

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-10jc7w38
Enrollment
Unknown
Registered
2022-09-02
Start date
2022-05-01
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

Tooth Diseases

Interventions

This study is a randomized clinical trial, with a split-mouth design with two arms (the same participant will receive the two interventions in different teeth), and double blind (participant and evalu
the cavities received Futurabond U universal adhesive (Voco) according to the manufacturer's recommendations. Then, the cavities will be restored with the protocols described below: The first arm will
E06.323.428

Sponsors

Universidade Estadual de Ponta Grossa
Lead Sponsor
Universidade Estadual de Ponta Grossa
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Good general health; good oral hygiene; have at least 20 teeth under occlusion; at least two comparable non-carious cervical lesion (in size; shape and dimensions); non-retentive; deeper than 0.5 mm; and involving both enamel and dentin of vital teeth; the cavo-superficial margin cannot involve more than 50% of the enamel.

Exclusion criteria

Exclusion criteria: Extremely poor oral hygiene; using orthodontic devices; severe or chronic periodontitis; heavy bruxism habits; known allergy to resin-based materials or any other material used in this study; pregnant or lactating women; chronic use of anti-inflammatory; analgesic and psychotropic drugs.

Design outcomes

Primary

MeasureTime frame
To evaluate color matching using a digital spectrophotometer on the performance of a composite resin with intelligent chromatic technology versus a traditional composite resin in non-carious cervical lesions. Interim data analyzes will be performed at 6, 12, 24, 36 and 60 months.

Secondary

MeasureTime frame
Evaluate the aesthetic properties; functional properties and biological properties using the World Dental Federation (FDI) clinical criteria on the performance of a composite resin with intelligent chromatic technology versus a traditional composite resin in non-carious cervical lesions. Interim data analyzes will be performed at 6, 12, 24, 36 and 60 months.

Countries

Brazil

Contacts

Public ContactAlessandro Loguercio

Universidade Estadual de Ponta Grossa

aloguercio@hormail.com+55 (42) 3220 3740

Outcome results

None listed

Source: REBEC (via WHO ICTRP)