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

Not Applicable

• Conditions: Tooth Cervix, Tooth Abrasion, Tooth Erosion, Tooth wear; A14.549.167.900.700; C07.793.818.124; C07.793.818.500; C07.793.818

• Registration Number: RBR-6w5gwh
• Lead Sponsor: niversidade Estadual Paulista

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-08-15
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruitment completed
• Sex: Not specified
• Target Recruitment: Not specified

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

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.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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.