Restorations of cavities near carious gingiva with single increment resi
- Conditions
- Cervical free lesions of cariesk03.2K03.1K03.0
- Registration Number
- RBR-5syh8r
- Lead Sponsor
- niversidade Estaudual do Oeste do Paraná
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Adults 18 to 60 years of age;
Lesions close to the gingival tissue present in structurally compromised posterior teeth (class V);
Absence of periodontal disease;
The teeth must have occlusal contact with the antagonist;
Possessing occlusal balance and absence of premature contacts.
Possessing active periodontal disease;
To have dental mobility in grades I, II and III;
Possess uncontrolled caries activity;
Xerostomia;
Being in orthodontic treatment;
Bearing mandibular temporal dysfunction;
History of systemic diseases with repercussion in the gingiva and periodontal tissues;
Adverse reaction history to any of the materials used in this study;
To have a parafunctional habit;
Use of myorelaxant apparatus;
Pregnancy or lactation.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Restorations will be clinically evaluated by the USPHS (United States Public Health Services) criteria described by Cvar and Ryge in 1971 (Table 3) in the initial, 6, 12, 18 and 24 month periods.<br>
- Secondary Outcome Measures
Name Time Method <br>The number of patients based on previous studies (Sartori et al., 2013) and the performance of the sampling test were based on an analysis of variance for a design of repeated measurements, as two experimental groups. Assuming an analysis power of 0.90, effect size of 0.25 and type I error of 0.05, with a duration over time, a total sample size of 15 restorations per group was defined. This project has not been implemented GPower 3.1.9.