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Evaluation of the Heating of a single-increment thermoviscous composite resin in dental restoration

Clinical evaluation of Different Forms of Heating in the performance of a bulk-fill thermoviscous composite resin in the restoration of non-carious cervical lesions

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-889c9qv
Enrollment
Unknown
Registered
2021-10-04
Start date
2021-06-01
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 is a split-mouth randomized clinical trial where 60 patients received 120 restorations. The same patient will receive both interventions. Crontrol group: 60 non-carious cervical lesions received
then they will be restored with thermoviscous bulk-fill composite based on nano-hybrid methacrylate (VisCalor bulk, Voco) will be placed in the Caps Dispenser (Caps Dispenser, Voco) and heated to 68°
then they will be restored with thermoviscous bulk-fill composite based on nano-hybrid methacrylate (VisCalor bulk, Voco) will be placed in the Caps dispenser/warmer (VisCalor Dispenser, Voco) and hea
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: Patients over 18 years of age, of both genders in good general health, good oral hygiene and having at least 20 teeth in occlusion. Present at least two non-carious cervical lesions comparable 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 the retention rate of different forms of heating a bulk fill thermoviscous resin in non-carious cervical lesions established by the World Dental Federation (FDI). Interim data analyzes will be performed at 6, 12, 18, 24 and 60 months.

Secondary

MeasureTime frame
To evaluate the surface gloss/luster and roughness; surface and marginal staining; marginal adaptation; color match; esthetic anatomical form; recurrence of initial pathology; tooth cracks and fractures; effect of the restoration on the periodontium; postoperative sensitivity; recurrence of caries; tooth Integrity; periodontal response and oral health of different forms of heating a bulk fill thermoviscous resin in non-carious cervical lesions established by the World Dental Federation (FDI). Interim data analyzes will be performed at 6, 12, 18, 24 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)