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Evaluation of the solvent Evaporation Time of universal adhesives in the quality of Cervical Lesions restorations

Not Applicable
Conditions
Tooth Abrasion
Tooth Attrition
Tooth 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
Inclusion Criteria

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.

Exclusion Criteria

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
NameTimeMethod
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
NameTimeMethod
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
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