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Clinical evaluation of a fluid material to cover tooth cavities with lesions close to the gum.

Clinical evaluation of Methacrylate and Ormocer® fluid composite resins in noncarious cervical lesions.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-998r5b
Enrollment
Unknown
Registered
2020-03-24
Start date
2019-08-01
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

Dental Caries

Interventions

Control Group: high viscosity restoration material (Admira Fusion Flow, Voco), 60 teeth. Experimental group 1: High viscosity flow restoration material (GrandioSO Heavy Flow, Voco), 60 teeth. Experi
Other
V03.175.250

Sponsors

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

Eligibility

Inclusion criteria

Inclusion criteria: Patients over 18 years old will be included; presence of at least two non-carious cervical lesions per patient regardless of their location in the dental arch; need of restorative treatment; adequate oral hygiene; absence of motor difficulties that prevent the performance of adequate oral hygiene; absence of periodontal disease active caries lesions and parafunctional habits; at least 20 teeth in function; absence of active removable partial denture clips on the teeth included in the research and that these are not prosthetic pillars; non-carious cervical lesions with a maximum of 50% enamel margin.

Exclusion criteria

Exclusion criteria: Under 18 years old; Patients who do not agree with the terms of the survey; Who do not feel motivated to participate in research and maintain oral hygiene; Who have difficulty attending the subsequent controls of the restoration.

Design outcomes

Primary

MeasureTime frame
Expected outcome: Number of restorations that fell after 6 and 12 months.

Secondary

MeasureTime frame
Marginal discoloration will be assessed on a scale from 1 to 5 proposed by the International Dental Federation (FDI method) after 6 and 12 months.;Marginal adaptation will be assessed on a scale of 1 to 5 proposed by the International Dental Federation (FDI method) after 6 and 12 months.;The caries lesion adjacent to the restoration will be assessed on a scale of 1 to 5 proposed by the International Dental Federation (FDI method) after 6 and 12 months.;Postoperative sensitivity will be assessed on a scale of 1 to 5 proposed by the International Dental Federation (FDI method) after 6 and 12 months.

Countries

Brazil

Contacts

Public ContactAlessandro Dourado Loguercio

Universidade Estadual de Ponta Grossa

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

Outcome results

None listed

Source: REBEC (via WHO ICTRP)