The effect of the release of composite resin components on restoration to gingival tissue

Not Applicable

Recruiting

• Conditions: periodontal disease ,Tooth Erosion,Tooth Attrition, Tooth Abrasion; C07.465.714; C07.793.818.500; C07.793.818.124; C07.793.818.249

• Registration Number: RBR-8m8cf2
• Lead Sponsor: niversidade Federal de Minas Gerais

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-06-13
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

Older than 18 years, systemically healthy, non-smoking, with good oral hygiene, with absence of irreversible pulpal alteration, with the presence of a non-carious cervical lesion (LCNCs) that needs to be restored, normal periodontium

Exclusion Criteria

With severe systemic alteration, in the use of antibiotics and anti-inflammatories in the last three months, with altered periodontium, non-smoking only, who have performed other restorations in the last 6 months, pregnant women and infants, periodontal sites that presented bleeding during crevicular fluid collection or sites that prevent adequate collection of clinical parameters

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Improved sensitivity of patients' teeth. Through a sensitivity test on the teeth before and after the restoration

Secondary Outcome Measures

Name	Time	Method
Retention rate of restorations made on non-carious cervic lesions. Data collected 10 minutes, 1 day, 7 days and one month after restorations