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Clinical Evaluation of Adhesives for Restoration of cavities in the Cervix of the Teeth not Caused by Caries

Randomized Clinical Evaluation of Simplified Adhesive Systems in Non-Carious Cervical Lesions: Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4rw55d
Enrollment
Unknown
Registered
2018-04-27
Start date
2014-08-10
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

Interventions

Participants will receive composite resin restorations in class V cavities (cavities in the cervix) from non-carious cervical lesions. There will be 152 restorations, divided into 4 groups (n = 38) ac
3M, ESPE, St.Paul, MN, USA): 37% phosphoric acid (Scotchbond ™ Etchant 37%, 3M, ESPE, St.Paul, MN, USA) will be applied to the dentin and enamel, washed with air/water jet 10 s, remove excess water wi
Kuraray, Japan): The primer will be applied actively. After drying the cavity for 5s and applying the adhesive, actively. The adhesives will be light-cured for 10s. 3. Universal adhesive system in th
Procedure/surgery
E06.323.428

Sponsors

Instituto de Ciência e Tecnologia - Universidade Estadual Paulista
Lead Sponsor
Instituto de Ciência e Tecnologia - Universidade Estadual Paulista
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Being in good general health; Be over 18 years of age; Have an acceptable level of oral hygiene; To present at least 20 teeth under occlusion; To have at least 4 non-carious lesions on different teeth to be restored. The lesions should be non-carious, non-retentive, with a depth greater than 1mm, and enamel and dentin envelopment of vital teeth without mobility; The cavo-superficial margin can not involve 50% more enamel.

Exclusion criteria

Exclusion criteria: Patients with extremely poor oral hygiene; Cronic or severe periodontitis; Severe parafunctional habits

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.;The presence of the fracture 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.

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

tacileo@uol.com.br+55-12-39479304

Outcome results

None listed

Source: REBEC (via WHO ICTRP)