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Restoration of cavities in the Cervix of the Teeth not Caused by Caries: clinical evaluation

Class V Non-Carious Cervical Lesions restorations with bioactive resins: randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5ktb2t
Enrollment
Unknown
Registered
2018-12-13
Start date
2018-08-16
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 Cervix, Tooth Abrasion, Tooth Erosion, Tooth wear

Interventions

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D05.750.716.822.308.300
Procedure/surgery
Participants will receive composite resin restorations in class V cavities (cavities in the cervix) from non-carious cervical lesions. There will be 60 restorations, divided into 2 groups (n = 30) acc

Sponsors

Instituto de Ciência e Tecnologia - ICT UNESP
Lead Sponsor
Instituto de Ciência e Tecnologia - ICT UNESP
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Be over 18 years of age; Being in good general health, Have an acceptable level of oral hygiene, To present at least 2 non carious cervical lesions in canines or premolars, Tooth vitality (tooth to be restored), antagonist tooth, availability to attend the evaluations

Exclusion criteria

Exclusion criteria: Present allergies to the materials employed, initiate the use of removable prothesis, braces or pregnancy during the study period

Design outcomes

Primary

MeasureTime frame
Retention failure of composite restorations will be evaluated by clinical assessment (visual inspection), considering a variation of at least 5% in the measurements after the intervention (7 days) and 24 months

Secondary

MeasureTime frame
The presence of the Marginal discoloration of the restoration will be evaluated by clinical assessment (visual inspection), considering a variation of at least 5% in the measurements after the intervention (7 days) and 24 months.;The presence of the recurrence caries will be evaluated by clinical assessment (visual inspection), considering a variation of at least 5% in the measurements after the intervention (7 days) and 24 months.

Countries

Brazil

Contacts

Public ContactTaciana Caneppele

Instituto de Ciência e Tecnologia - Universidade Estadual Paulista

taciana@ict.unesp.br+55-012-39479304

Outcome results

None listed

Source: REBEC (via WHO ICTRP)