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Clinical evaluation of a universal material to cover tooth wear close to the gum before and after in-office whitening

Universal composite resin color compatibility before and after in-office whitening

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4wrk7dy
Enrollment
Unknown
Registered
2025-02-05
Start date
2025-02-01
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

Composite Resins

Interventions

This is a randomized, double-blind clinical study. Experimental group: 42 participants with two non-carious cervical lesions side by side will undergo the interventions (42 non-carious cervical lesion
the cavities will receive Futurabond U adhesive according to the manufacturer's recommendations. Then, the cavities will be restored with the protocols described below: one with Admira Fusion X-tra an
E06.420.750

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: Minimum age of 18 years; both genders; good oral hygiene; present at least 20 teeth under occlusion; at least two non-carious cervical lesions comparable in size, shape and dimensions; non-retentive; deeper than half a millimeter; involve both the enamel and dentin of vital teeth; the cavosurface margin cannot involve more than 50% of the enamel

Exclusion criteria

Exclusion criteria: Extremely poor oral hygiene; wearing orthodontic appliances; 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 drugs; analgesics and psychotropic drugs

Design outcomes

Primary

MeasureTime frame
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 immediate and 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 immediate and 6, 12, 24, 36 and 60 months.

Countries

Brazil

Contacts

Public ContactMichael Favoreot

Universidade Estadual de Ponta Grossa

michaelfavoreto@hotmail.com+55 (42) 999607607

Outcome results

None listed

Source: REBEC (via WHO ICTRP)