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Clinical evaluation of a monochromatic composite resin of dental restoration

Clinical evaluation of a monochromatic composite resin

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-8txr4fw
Enrollment
Unknown
Registered
2022-05-26
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

Sixty participants with two non-carious cervical lesions side by side will undergo the interventions. Randomization will be done intra-individual so that each subject receives two restorations, one fr
the wells received Ambar Universal Adhesive (FGM) according to the manufacturer's recommendations. Then, the cavities will be restored with the protocols described below: Vittra Unique
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 match using a digital spectrophotometer on the performance of a monochromatic composite versus a traditional composite 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 monochromatic composite versus a traditional composite 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) · Data processed: Feb 6, 2026