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Evaluation of a bulk-fill thermoviscous composite resin in dental restoration

Clinical evaluation of a thermoviscous bulk-fill composite restorations in non-carious cervical lesions

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6d6gxxz
Enrollment
Unknown
Registered
2021-10-11
Start date
2021-05-01
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

Stomatognathic Diseases

Interventions

CONTROL GROUP: 60 non-carious cervical lesions were cleaned and isolated using portrait wire and the universal adhesive system (Futurabond U,Voco) applied in self-etching mode associated with selectiv
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 LCNCs (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
Clinically evaluate the performance retention rate of a bulk-fill thermoviscous composite resin versus a regular resin in LCNCs. Interim data analyzes will be performed at 6, 12, 18, 24 and 60 months.—

Secondary

MeasureTime frame
Clinically evaluate the performance of a bulk-fill thermoviscous composite resin versus a regular resin in NCCLs using the World Dental Federation (FDI) clinical criteria. Interim data analyzes will be performed at 6, 12, 18, 24 and 60 months.—

Countries

Brazil

Contacts

Public ContactAlessandro;MICHAEL Loguercio;FAVORETO

Universidade Estadual de Ponta Grossa;Universidade Estadual de Ponta Grossa

aloguercio@hormail.com;michaelfavoreto@hotmail.com+55 (42) 3220 3740;+55(42)32203740

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 8, 2026