Clinical evaluation of a Monochromatic Flow Composite Resin of dental restoratio

Not Applicable

Recruiting

• Conditions: Tooth Diseases; C07.793.818.124

• Registration Number: RBR-5hs9prz
• Lead Sponsor: niversidade Estadual de Ponta Grossa

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-10-24
• Last Update Posted: 13 November 2023
• Study Completion: 2027-08-01

Recruitment & Eligibility

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

Inclusion Criteria

Good general health;good oral hygiene;present at least 20 teeth under occlusion;at least two non-carious cervical lesions comparable in size;format and dimensions;non-retentive;deeper than half a mm;and involve both the enamel and dentin of vital teeth;The cavo-superficial margin cannot involve more than 50% of the enamel

Exclusion Criteria

Extremely poor oral hygiene;using orthodontic devices;severe or chronic periodontitis;heavy bruxism habits;known allergy to resin-based materials or any other material used in this study;pregnant or lactating women;chronic use of anti-inflammatory;analgesic and psychotropic drugs

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Evaluate color match using a digital spectrophotometer on the performance of a monochromatic composite versus a traditional composite in non-carious cervical lesions. Interim data analyzes will be performed immediate and 6, 12, 24, 36 and 60 months.

Secondary Outcome Measures

Name	Time	Method
Evaluate the aesthetic properties; functional properties and biological properties using the World Dental Federation (FDI) clinical criteria on the performance of a monochromatic composite versus a traditional composite in non-carious cervical lesions. Interim data analyzes will be performed immediate and 6, 12, 24, 36 and 60 months.