Evaluation of the solvent Evaporation Time of universal adhesives in the quality of Cervical Lesions restorations
- Conditions
- Tooth AbrasionTooth AttritionTooth Erosion
- Registration Number
- RBR-2hbf2mx
- Lead Sponsor
- niversidad de los Andes, Chile
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Patients older than 18 years will be included; Presence of at least two Non-Carious Cervical Lesions per patient regardless of their location in the dental arch; With a need for restorative treatment; acceptable level of oral hygiene according to the Simplified Oral Hygiene Index; Absence of driving difficulties that prevent adequate oral hygiene; Absence of periodontal disease active caries lesions and parafunctional habits; At least 20 teeth in function; Absence of active staples of removable partial dentures on the teeth included in the research and that these are not pillars of prostheses; Non-Carious Cervical Lesions with a maximum of 50% of enamel margin.
Under 18 years old; Patients who do not agree with the terms of the study; Who do not feel motivated to participate in research and maintain oral hygiene; Who have difficulty attending the subsequent controls of the restoration.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method It is expected to find a 10% decrease in retention criteria, in restorations where a solvent evaporation of 5 seconds was carried out, compared to the restorations where a solvent evaporation of 25 seconds was carried out, evaluated by means of the criteria of clinical evaluation of the International Dental Association (FDI), at 12 months
- Secondary Outcome Measures
Name Time Method It is expected to find a 20% increase in criteria 3 and 4 (clinically satisfactory and clinically unsatisfactory) of marginal adaptation in restorations where a solvent evaporation of 5 seconds was carried out, compared to the restorations where a solvent evaporation of 25 seconds was carried out, evaluated by means of the criteria of clinical evaluation of the International Dental Association (FDI), at 12 months;It is expected to find a 20% increase in criteria 3 and 4 (clinically satisfactory and clinically unsatisfactory) of marginal staining in restorations where a solvent evaporation of 5 seconds was carried out, compared to the restorations where a solvent evaporation of 25 seconds was carried out, evaluated by means of the criteria of clinical evaluation of the International Dental Association (FDI), at 12 months