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Clinical evaluation of non-carious cervical lesions of different sizes, restored with two resin composite

Longitudinal clinical evaluation of non-carious cervical lesions of different sizes, restored with bulk-fill or conventional resin composite: randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6w5gwh
Enrollment
Unknown
Registered
2017-08-15
Start date
2016-08-08
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

Participants will receive restorations in class V cavities from non-carious cervical lesions, previously classified according to the extent of the cavity in the cervico-occlusal direction. There will
• Regular bulk-fill resin. 2. Extension of the cavity of the non-carious cervical lesion, on two levels:         • Extension 1.5 mm ± 10%.         • Extension 3 mm ± 10%. Restoration of the lesions w
Procedure/surgery
E06.323.428
D05.750.716.822.308

Sponsors

Universidade Estadual Paulista
Lead Sponsor
Universidade Estadual Paulista
Collaborator

Eligibility

Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: At least 18yrs old; good health; do not have active caries or periodontal disease; to have non carious cervical lesions, in canines and premolars, at least 1 mm depth; to have at least 1 lesion; to have antagonist and adjacent teeth; teeth must to present vital pulp; no parafunctional habits.

Exclusion criteria

Exclusion criteria: Medical condition that may interfere with the safety of the volunteer during the study period, or allergic reactions to the substances and / or products will be used; use of removable prostheses which have the clamps resting on the teeth used for the research; parafunctional habits; smoking patients.

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
Presence of fractures , marginal desadaptation, marginal discoloration, postoperative sensitivity and tooth caries recurrence will be evaluated in the composite restorations 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 - ICT UNESP

taciana@fosjc.unesp.br+55 1239479304

Outcome results

None listed

Source: REBEC (via WHO ICTRP)