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Effect of occlusal factors on clinical performance in the restorative treatment of cervical lesions non-carious

Effects of occlusal factors on the clinical performance of restorations in non-carious cervical lesion

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7t5nqgm
Enrollment
Unknown
Registered
2022-11-01
Start date
2022-06-01
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 abrasion

Interventions

This is a double-blind, randomized controlled clinical trial, four armed. There will be a random division into four groups using sealed envelopes. Each group will have at least 30 restorations, divide
Group B: restoration with flowable resin and no occlusal adjustment
Group C: restoration with conventional resin and with occlusal adjustment and Group D: restoration with conventional resin and without occlusal adjustment. This division aims to investigate whether or

Sponsors

Pontíficia Universidade Católica do Paraná
Lead Sponsor
Pontíficia Universidade Católica do Paraná
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Good general health; good level of oral hygiene; of age (18 years); having at least two non-carious cervical lesions; presence of occlusal interference; depth of lesions of at least 1mm

Exclusion criteria

Exclusion criteria: Active or chronic periodontitis; bruxism and dental clenching; orthodontic treatment in progress; performance of tooth whitening during the last 6 months; pregnancy and/or lactation; endodontic treatment in the tooth with a non-carious cervical lesion; carious cervical lesion; absence of antagonist tooth in teeth with non-carious cervical lesion

Design outcomes

Primary

MeasureTime frame
It is expected to identify whether the effects of occlusal factors affect the clinical performance of restorations in non-carious cervical lesions, through clinical follow-ups based on the modified USPHS criteria, which will measure the following parameters of restorations: anatomical shape, surface roughness, marginal discoloration, retention, marginal adaptation, postoperative sensitivity, secondary caries and fracture.

Secondary

MeasureTime frame
It is expected to identify whether restorations in non-carious cervical lesions performed in conventional composite resin present the same clinical performance as those performed in fluid composite resin, through the parameters measured by the modified USPHS.

Countries

Brazil

Contacts

Public ContactJullyana Mayara Dezanetti

Pontíficia Universidade Católica do Paraná

ju_preizner@hotmail.com+55(41)999668240

Outcome results

None listed

Source: REBEC (via WHO ICTRP)